21571632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141562-A-G

21571674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141534-A-G

21571750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141465-T-C

http://identifiers.org/hco/7/GRCh38#21571753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118141462-A-C

21571753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141462-A-G

21571790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141421-T-C

21571793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141394-G-A

21571800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118141387-A-G

21571800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118141387-A-T

21571860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 118141327-G-A

21571965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 118141222-A-G

21571980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118141207-T-G

http://identifiers.org/hco/7/GRCh38#21572002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118141188-C-A

21572002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141188-C-G

21572002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141188-C-T

21572003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141187-A-G

21572003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141187-A-T

21572004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141186-T-A

http://identifiers.org/hco/7/GRCh38#21572043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118141146-C-A

21572043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141146-C-G

21572205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141007-G-A

21572225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118140991-T-C

http://identifiers.org/hco/7/GRCh38#21572795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118140451-A-C

21572795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118140451-A-G

21572802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118140444-C-T

21578799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118124616-A-G

21578846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118124570-A-G

http://identifiers.org/hco/7/GRCh38#21578883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118124535-A-C

21578883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118124535-A-G

21578948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118124476-A-G

21578966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118124458-A-G

21579332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118124094-G-C

21579710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118123802-A-G

21579804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118123735-G-C

21579809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118123729-T-C

21579809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118123729-T-G

21579977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118123587-G-A

21580133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118123264-A-G

21580447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118122762-A-G

21580532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118122669-T-C

21581087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118121915-C-T

21581238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118121788-C-T

http://identifiers.org/hco/7/GRCh38#21581293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118121724-A-C

21581446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118121574-G-A

21581446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118121574-G-T

21581639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118121401-G-C

21581667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118121388-A-G

21581774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118121307-T-C

http://identifiers.org/hco/7/GRCh38#21581782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118121294-A-C

21581786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118121290-A-G

21581843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118121190-G-A

21581843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118121190-G-T

21581971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118121064-A-G

http://identifiers.org/hco/7/GRCh38#21582153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118120890-C-A

21582153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118120890-C-G

21582300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118120739-A-G

http://identifiers.org/hco/7/GRCh38#21582555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118120481-C-A

21582555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118120481-C-T

21582653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118120277-T-A

21584639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118119910-T-A

21584646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118119906-C-T

21584842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118119712-T-G

21584855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118119647-A-T

21584882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118119618-A-G

21584908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118119585-G-C

21584929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118119564-T-C

21585102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118119377-T-C

21585202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118119289-C-T

21585230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118119268-G-A

21585233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118119265-C-T

21585272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118119226-G-A

http://identifiers.org/hco/7/GRCh38#21585644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118118965-A-C

21585706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118112128-T-C

21585780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118112066-A-G

21585895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118111965-G-C

21585941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118111915-T-G

21586057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118111827-A-G

21586252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118111685-C-G

21586323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118111610-G-A

21586456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118111482-G-A

http://identifiers.org/hco/7/GRCh38#21586514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118111429-A-C

21586543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118111400-C-G

21586557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118111386-T-A

21586557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118111386-T-C

21586598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118111348-T-C

21586681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118111264-C-T

21586762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118111227-G-C

http://identifiers.org/hco/7/GRCh38#21586959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118107675-C-A

21586959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118107675-C-G

21586959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118107675-C-T

21586975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118107659-A-G

21587237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118107425-C-T

21587240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118107422-C-G

21587240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118107422-C-T

21587277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118107391-T-C

21587345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118107310-G-T

21587355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118107305-T-C

http://identifiers.org/hco/7/GRCh38#21587409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118107269-A-C

21587554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118107109-A-G

21587621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118107048-A-G

21587879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106839-T-G

21588077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118106649-T-G

21588301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106387-G-A

21588301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106387-G-C

21588317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106293-G-A

21588317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106293-G-C

21588317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106293-G-T

21588327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106283-A-G

21588327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106283-A-T

http://identifiers.org/hco/7/GRCh38#21588336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118106275-C-A

21588336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106275-C-G

http://identifiers.org/hco/7/GRCh38#21588395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118106217-A-C

21588410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106203-T-C

21588455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106161-A-G

21588460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106156-A-T

21588461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106155-T-C

21588461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106155-T-G

21588463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118106153-C-T

21588693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118105779-A-G

21588791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118105685-G-A

http://identifiers.org/hco/7/GRCh38#21588879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118105600-C-A

21589009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118105483-A-G

21589212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118104496-T-C

21589317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118104391-G-A

21589317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118104391-G-T

21589473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118104223-A-G

21589511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118104178-G-A

http://identifiers.org/hco/7/GRCh38#21589522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118104167-A-C

21589522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118104167-A-G

21589543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118104147-G-T

21589578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118103843-C-T

http://identifiers.org/hco/7/GRCh38#21589844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118103555-A-C

21589913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118103489-G-A

21590346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118102726-G-C

21590385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118102699-T-G

21590534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118102564-T-G

21590590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118102509-A-G

21590617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118102481-C-T

21590620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118102478-C-G

21590813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118095570-A-G

21590814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118095569-T-C

http://identifiers.org/hco/7/GRCh38#21590837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118095547-A-C

21590837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118095547-A-T

21590884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118095143-A-G

21590886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118095141-A-G

21591130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118094911-A-G

21591132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118094909-A-G

21591169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118094860-G-C

21591232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118094797-A-G

21591300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118094729-C-G

21591363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118094666-C-T

21591374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118094655-G-A

21591374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118094655-G-C

21591412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118094617-G-A

21591412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118094617-G-T

http://identifiers.org/hco/7/GRCh38#21591413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118094616-A-C

21591500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118094529-G-A

21591600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118094429-G-A

21591610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118094419-T-A

21591610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118094419-T-G

21599319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118091947-T-C

21599429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118091840-G-A

http://identifiers.org/hco/7/GRCh38#21599766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118091533-C-A

21599766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118091533-C-G

21599766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118091533-C-T

21599881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118091421-A-G

21599938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118091364-C-T

21599954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118091348-A-G

http://identifiers.org/hco/7/GRCh38#21600127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118091175-C-A

21600127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 118091175-C-G

21600127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 118091175-C-T

21600539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118091134-G-T

21600541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118091132-T-C

21600570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118091101-C-G

21600572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118091080-A-G

21600599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118091054-T-G

21600652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118091018-G-C

21600757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118090913-T-C

21600846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118090824-T-C

21600846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118090824-T-G

http://identifiers.org/hco/7/GRCh38#21600880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118090790-A-C

21600936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118090737-G-A

21600940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118090733-A-G

21600948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118090725-C-T

21600952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118090721-T-C

21601412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118089678-G-A

21601412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: stop gained
orthologous variants: 118089678-G-T

21601460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118089630-G-A

21601556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118089534-A-G

21601637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118089455-T-A

21601656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118089436-T-C

21601656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118089436-T-G

21601690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118089402-A-T

http://identifiers.org/hco/7/GRCh38#21601706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118089391-C-A

21601706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118089391-C-T

21601965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118089170-T-A

21601965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118089170-T-C

21602273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118088833-A-G

21602884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118088288-G-T

21603247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118088014-T-C

21603286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118087974-C-T

21603373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118087898-G-T

21603407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118087864-T-G

21603413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118087856-G-A

21603478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118087791-C-T

http://identifiers.org/hco/7/GRCh38#21603545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118087727-A-C

http://identifiers.org/hco/7/GRCh38#21603611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118087664-A-C

http://identifiers.org/hco/7/GRCh38#21603725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118087565-C-A

21603811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118087300-T-C

21603894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118087213-T-C

21604028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118087081-T-A

21604230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118086846-C-T

21604358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118086717-C-T

21604415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118086662-T-A

21604462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118086620-G-A

21604765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118086451-A-G

21604893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118086195-A-G

21604936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118086154-T-A

21604949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118086141-C-T

21605025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118086068-T-C

21605239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118085850-A-G

21605327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118085759-T-C

21605327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118085759-T-G

21605346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118085747-G-C

21605587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118085536-C-G

21605588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118085535-C-T

21605781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118085194-T-A

21606285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118084640-T-C

21606330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118084593-A-G

21606414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118084517-T-C

21606498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118084437-A-G

21606507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118084428-G-A

21606570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118084356-A-G

21606739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118084200-A-G

21606760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118084180-T-A

21608491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118081606-C-G

21608714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118081410-G-A

21608714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118081410-G-T

21608783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118081331-G-C

21608808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118081307-C-T

21608866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118081245-T-C

21608893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118081218-T-C

21609071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118081043-G-A

21609187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118080991-C-T

21609807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118080302-T-G

21609845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118080252-G-C

21609880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118080220-G-C

21609915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118080180-A-G

21609941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118080154-T-A

21609965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118080131-A-G

21610173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118080100-G-C

http://identifiers.org/hco/7/GRCh38#21610451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118079950-C-A

21610451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118079950-C-T

21610457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118079944-G-A

21610515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118079881-A-G

21610746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118079658-G-C

21610902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118079514-T-G

http://identifiers.org/hco/7/GRCh38#21614514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118078530-A-C

http://identifiers.org/hco/7/GRCh38#21615008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118077775-C-A

21615008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077775-C-T

21615030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077754-A-G

21615035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077745-G-A

21615035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077745-G-C

21615035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077745-G-T

http://identifiers.org/hco/7/GRCh38#21615059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118077721-C-A

21615059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077721-C-T

21615085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077719-G-A

21615085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077719-G-C

21615085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077719-G-T

21615091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077713-A-G

21615091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077713-A-T

21615100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077708-T-A

21615126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118077682-C-G

21615126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118077682-C-T

21615164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118077644-A-G

21615243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118077565-G-C

21615296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077515-T-A

http://identifiers.org/hco/7/GRCh38#21615321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118077484-C-A

21615321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077484-C-G

http://identifiers.org/hco/7/GRCh38#21615352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118077462-A-C

21615352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077462-A-G

21615355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077459-T-C

http://identifiers.org/hco/7/GRCh38#21615378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118077436-A-C

21615378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077436-A-G

21615417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077384-T-C

21615454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077352-T-C

21615517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077285-C-T

21615550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077257-T-C

21615581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077226-T-C

21615590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077217-C-T

21615658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118077155-T-G

http://identifiers.org/hco/7/GRCh38#21615701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118077111-A-C

21615912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118076900-C-T

21616089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118076722-T-C

21616126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118076685-G-A

21616304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118076510-A-G

http://identifiers.org/hco/7/GRCh38#21616312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118076502-A-C

21616312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118076502-A-G

http://identifiers.org/hco/7/GRCh38#21616382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118076434-C-A

21616404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118076412-A-G

21616425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118076391-G-T

21616693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118076125-C-T

21616785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118076033-A-G

21616825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118076005-C-T

21616928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118075792-C-G

http://identifiers.org/hco/7/GRCh38#21616929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118075791-C-A

21617121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 118075621-C-T

21617124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 118075618-G-A

21617137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 118075606-C-T

21617171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 118075563-A-G

21617184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 118075550-T-G

http://identifiers.org/hco/7/GRCh38#21617203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#118075532-A-C

21617203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 118075532-A-G

21617249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 118075489-G-A

http://identifiers.org/hco/7/GRCh38#21617329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#118075425-C-A

21617329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 118075425-C-T

21617373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 118075390-G-A

21617424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118075339-T-G

21617472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118075292-T-C

21617476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118075164-G-A

21617476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118075164-G-T

http://identifiers.org/hco/7/GRCh38#21617491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118075042-C-A

21617491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118075042-C-T

21617496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118075037-A-G

21617496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118075037-A-T

http://identifiers.org/hco/7/GRCh38#21617506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118075027-C-A

21617506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118075027-C-G

21617563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118074859-T-G

21617593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118074835-A-G

21617599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118074829-T-C

21617646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118074783-C-G

21617646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118074783-C-T

21617823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118074609-G-A

21617823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118074609-G-C

21617836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 118074597-G-T

21617848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 118074585-T-A

21617848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 118074585-T-C

21617857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118074576-G-C

21618355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118074329-G-T

21618356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118074328-G-A

21618418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118074270-T-C

21618433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118074255-T-C

http://identifiers.org/hco/7/GRCh38#21618459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118074230-C-A

21618459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118074230-C-T

21618513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118074178-A-G

http://identifiers.org/hco/7/GRCh38#21618935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118073787-A-C

21618935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118073787-A-G

21619172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118073634-G-A

http://identifiers.org/hco/7/GRCh38#21619197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118073609-C-A

21619197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118073609-C-T

21619240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118073566-G-C

21619255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118073551-G-T

21619340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118073473-T-A

http://identifiers.org/hco/7/GRCh38#21619358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118073459-A-C

21619358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118073459-A-G

21619358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118073459-A-T

21619365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118073454-G-A

21619365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118073454-G-C

21619365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118073454-G-T

21619551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118073271-A-T

21619595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118073227-C-G

21619726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118073068-C-G

21619856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118072937-T-C

http://identifiers.org/hco/7/GRCh38#21619914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118072819-C-A

21619914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118072819-C-G

21619914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118072819-C-T

21620064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118072663-C-G

21620101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118072632-A-G

21620101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118072632-A-T

http://identifiers.org/hco/7/GRCh38#21633863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118072015-A-C

21634090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118071786-C-T

21634263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118071635-A-G

21634308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118071597-C-G

21634310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118071595-A-G

21634413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118071507-C-T

21634464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118071465-T-A

21635060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118071344-A-T

21635086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118071318-A-G

21635399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118070754-G-A

21635399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118070754-G-C

21635399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118070754-G-T

21635434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118070717-G-A

21635534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118070632-A-G

http://identifiers.org/hco/7/GRCh38#21635826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118070397-C-A

21635826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118070397-C-G

21635826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118070397-C-T

21635955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118070274-G-A

21636019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118070210-T-C

21636103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 118070126-A-G

21636103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 118070126-A-T

21636162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118070077-G-A

21636162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118070077-G-T

21636334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118069903-T-C

21637473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118069852-T-C

21637473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118069852-T-G

http://identifiers.org/hco/7/GRCh38#21637498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118069828-C-A

21637498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118069828-C-T

21637553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118069777-T-G

21637714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118069624-G-A

21637714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118069624-G-T

21638188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118069063-A-G

21638549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068865-G-A

21638790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068707-A-T

21638807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068698-A-G

http://identifiers.org/hco/7/GRCh38#21638854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118068661-A-C

21638854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068661-A-G

21638924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068608-T-C

21639074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068462-T-C

21639074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068462-T-G

21639135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068405-G-A

21639135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068405-G-T

21639165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068375-C-T

21639362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068241-G-T

21639364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068239-A-G

21639571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068197-A-G

21639639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118068129-T-C

21639902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118067894-A-G

21639911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118067888-G-T

http://identifiers.org/hco/7/GRCh38#21639912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118067887-C-A

21639912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118067887-C-G

21639977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118067811-C-T

21640142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118067658-T-A

21640142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118067658-T-G

21640222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118067593-C-G

21640315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118067492-C-T

21640367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118067457-G-A

http://identifiers.org/hco/7/GRCh38#21640398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118067434-A-C

21640495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118067343-G-T

21640685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118067166-C-T

21640694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118067157-A-G

21640776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118067077-T-G

21640929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118066898-C-T

21641220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118066342-C-G

21641220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118066342-C-T

21641254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118066308-T-C

21641254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118066308-T-G

http://identifiers.org/hco/7/GRCh38#21641273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118066290-A-C

21641273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118066290-A-T

21641374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118066199-A-T

21641375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118066198-C-G

21641375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118066198-C-T

21641376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118066197-T-G

http://identifiers.org/hco/7/GRCh38#21641438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118065572-C-A

21641438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118065572-C-T

21641643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118065205-T-A

21641667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118065183-A-G

21641676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118065174-A-G

21641763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118065088-C-G

21641763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118065088-C-T

21641788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118065066-C-T

21641959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118064887-A-G

21642300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118064002-A-G

21642347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118063939-G-A

http://identifiers.org/hco/7/GRCh38#21642393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118063908-A-C

21642458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 118063850-T-C

http://identifiers.org/hco/7/GRCh38#21642526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#118063778-A-C

http://identifiers.org/hco/7/GRCh38#21642873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118063442-A-C

21642962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118063355-T-G

21643065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118063275-T-C

http://identifiers.org/hco/7/GRCh38#21643104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118063237-C-A

21643227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118063122-T-C

21643269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118063091-G-T

21643422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118062955-T-C

21643493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118062840-C-T

21643513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118062821-C-T

21643660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118062704-T-C

21643724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118062651-A-G

http://identifiers.org/hco/7/GRCh38#21643966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118062415-A-C

21644060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118062336-C-T

21644245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118062152-G-C

21644770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118062016-T-C

21644851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118061937-C-G

21644877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118061914-A-T

http://identifiers.org/hco/7/GRCh38#21645009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118061794-C-A

21645244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118061630-A-G

21645443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118061424-G-C

http://identifiers.org/hco/7/GRCh38#21645472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118061395-A-C

21645796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118061170-T-G

21645907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118061058-A-G

21646006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118060981-A-G

21646180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118060630-C-G

21646300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118060520-C-T

21646372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118060478-G-T

21646380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118060470-A-G

21646551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118060357-A-G

21646629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118060282-A-G

21646641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118060269-C-T

21647845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118059451-A-G

21648120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118059214-A-G

21648364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118059014-A-G

21648364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118059014-A-T

21648595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118058797-C-G

21648608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118058784-C-G

http://identifiers.org/hco/7/GRCh38#21648847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118058516-A-C

21649051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118058330-G-A

http://identifiers.org/hco/7/GRCh38#21649052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118058329-A-C

21650979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118057009-C-G

21650993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118056995-G-T

21651053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118056922-G-T

21651086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118056892-A-G

http://identifiers.org/hco/7/GRCh38#21651112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118056878-A-C

21651163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118056839-A-G

21651180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118056822-G-C

21651244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118056767-C-T

http://identifiers.org/hco/7/GRCh38#21651268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118056743-A-C

21651285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118056729-A-G

21651583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118056608-T-A

http://identifiers.org/hco/7/GRCh38#21651728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118056513-A-C

21651832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118056416-C-G

21652176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118056074-G-A

http://identifiers.org/hco/7/GRCh38#21652228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118056021-A-C

http://identifiers.org/hco/7/GRCh38#21652429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118055811-C-A

21652429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118055811-C-G

21652429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118055811-C-T

http://identifiers.org/hco/7/GRCh38#21652578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118055662-A-C

21653012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118055105-T-G

21653379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118054807-G-A

21653379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118054807-G-T

21653493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118054686-A-G

21653684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118054493-A-G

21653685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118054492-T-A

21653843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118054337-G-T

21653884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118054301-T-C

21653909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118054282-A-G

21653984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118054231-A-T

21653986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118054229-T-C

21653986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118054229-T-G

21654067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118054153-G-A

21654068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118054152-C-G

http://identifiers.org/hco/7/GRCh38#21654446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118051210-C-A

21654446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118051210-C-T

21654558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118051112-A-G

21654649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118051045-A-T

21654672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118051022-C-G

21654694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118051010-G-A

21654963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118050770-T-C

21655174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118050597-A-G

21655304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118050490-G-A

21655323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118050471-T-C

21655323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118050471-T-G

21655333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118050461-A-G

21655418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118050373-T-C

21655654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118049702-A-G

http://identifiers.org/hco/7/GRCh38#21655763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118049602-C-A

21655763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118049602-C-T

21655805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118049560-T-C

21655868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118049497-G-A

21655961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118049404-G-A

21655961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118049404-G-C

21655961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: stop gained
orthologous variants: 118049404-G-T

21655985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118049380-A-G

21655999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118049366-G-C

21655999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118049366-G-T

21656048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118049325-T-A

21656048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118049325-T-C

21656122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118049259-T-C

21656253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118049132-T-A

21656515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118048942-C-G

21656515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118048942-C-T

http://identifiers.org/hco/7/GRCh38#21657096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118047969-C-A

21657096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118047969-C-T

21657100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118047965-T-C

http://identifiers.org/hco/7/GRCh38#21657168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118047890-A-C

21657168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118047890-A-T

21657235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118047819-T-A

21657237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118047812-T-G

21657288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118047785-G-A

21657372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118047692-T-A

21657486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118047577-C-G

21657561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118047515-C-T

21657589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118047487-C-T

21657689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118047391-G-C

21658027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118047128-T-C

http://identifiers.org/hco/7/GRCh38#21658029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118047126-A-C

21658187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046977-G-T

21658322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046841-T-A

21658322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046841-T-C

21658324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046839-G-T

21658406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046756-A-G

21658406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046756-A-T

21658464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046707-G-A

21658465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046706-G-A

21658606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046580-C-T

http://identifiers.org/hco/7/GRCh38#21658660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118046528-C-A

21658660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046528-C-T

21658663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046525-T-G

http://identifiers.org/hco/7/GRCh38#21658766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118046428-C-A

21658766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046428-C-T

21659042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046153-G-T

21659046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046149-T-G

21659991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118046070-A-G

21660335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118045879-C-T

21660341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118045873-T-C

21660379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118045839-A-G

21660460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118045782-G-T

21660526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118045710-A-T

21660653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118045614-A-T

21660674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118045607-T-G

21660699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118045586-A-G

21660781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118045513-A-G

21660786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118045508-T-G

21663651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118045097-T-G

21663664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118045084-A-T

21663748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118044998-C-T

21663977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118044797-T-C

21664052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118044722-C-T

21664116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118044630-A-G

21664116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118044630-A-T

21664144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118044603-T-C

21664745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118043882-G-C

21664771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118043856-A-T

21664775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118043852-T-C

21664970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118043626-C-G

21664975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118043622-C-T

21665022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118043566-C-T

21665026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118043562-C-G

21665062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118043532-C-G

21665111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118043487-C-T

21665114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118043484-T-G

http://identifiers.org/hco/7/GRCh38#21665178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118043418-A-C

21665178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118043418-A-G

21665577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118043103-A-G

21665812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118042594-A-G

21665839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118042568-A-G

21665849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118042560-T-C

http://identifiers.org/hco/7/GRCh38#21665851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118042558-C-A

21665851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118042558-C-T

21665861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118042548-C-T

21665863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118042546-T-C

21665864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118042545-T-A

21665864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118042545-T-C

21665864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118042545-T-G

21665986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118042095-T-G

http://identifiers.org/hco/7/GRCh38#21666036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118042046-A-C

21666155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118041937-G-A

21666173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118041919-A-T

21675384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118037182-A-G

http://identifiers.org/hco/7/GRCh38#21675460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118037103-A-C

21675586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118036992-A-G

21675906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118036675-G-A

21675922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118036660-T-A

21675922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118036660-T-G

21676207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118036420-C-T

21676314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118036342-T-C

21676978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118035644-G-C

21676996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118035625-G-A

21677039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118035583-A-T

21677905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118035330-C-T

21678429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118034751-A-G

http://identifiers.org/hco/7/GRCh38#21678592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118034603-A-C

21678594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118034601-A-T

http://identifiers.org/hco/7/GRCh38#21678685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118034511-C-A

http://identifiers.org/hco/7/GRCh38#21679018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118034277-A-C

21679018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118034277-A-T

21679204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118034108-A-G

21679697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118033410-C-G

21679697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118033410-C-T

21679711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118033395-A-G

21679774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118033343-A-G

21679774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118033343-A-T

21679818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118033300-C-T

21680083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118033027-A-G

21680083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118033027-A-T

21680105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118033005-C-G

21680166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118032963-T-C

21680237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118032919-C-T

21680326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118032832-G-A

21680326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118032832-G-C

21680340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118032818-A-G

21680570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118032533-A-G

21680632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118032480-A-G

21680655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118032457-C-T

21680915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118032212-T-G

21681054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118032072-C-G

21681502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118031940-T-A

21681502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118031940-T-C

21681525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118031914-T-A

21681526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118031913-T-A

21681526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118031913-T-C

21681630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118031809-A-G

21681821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118031659-G-A

21681821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118031659-G-T

21681842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118031640-A-G

21681848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118031634-T-A

21681848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118031634-T-G

21682586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118030264-G-A

21682586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118030264-G-C

http://identifiers.org/hco/7/GRCh38#21682591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118030259-A-C

21682810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118029009-T-A

21683228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118028198-A-G

http://identifiers.org/hco/7/GRCh38#21683746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118027722-C-A

21683746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118027722-C-T

http://identifiers.org/hco/7/GRCh38#21683753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118027715-C-A

21683753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118027715-C-T

21683826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118027642-C-T

21683849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118027619-A-G

21683947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118027521-A-G

http://identifiers.org/hco/7/GRCh38#21683949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118027519-C-A

21683949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118027519-C-G

21684166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118027230-C-T

21684211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118027202-C-T

21684255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118027164-A-T

21684707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118026550-C-G

21684951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118026322-A-G

21685076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118026221-C-T

21685108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118026189-T-G

21685180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118026144-A-T

21685206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118026123-A-T

21685315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118026032-T-A

21685361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118025990-A-G

21685474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118025883-T-C

21685514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118025829-T-A

21685591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118025749-G-A

21685640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118025675-T-G

21685904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118025257-T-G

21686053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118025198-T-C

21686054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118025197-G-T

21686103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118025145-A-G

21686157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118025102-A-G

21686158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118025101-G-A

21686160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118025099-A-T

21686240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118025020-T-G

21686414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118024862-C-T

21686466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118024802-T-A

21686466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118024802-T-G

21686729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118024526-C-G

21686768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118024488-C-T

21686915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118024344-A-G

21687022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118024262-T-C

21687034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118024244-T-C

21687044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118024235-G-A

21687047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118024232-T-G

21687064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118024216-T-C

21687190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118024092-G-C

21687208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118024074-G-T

21687232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118024050-T-A

21687232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118024050-T-C

21687324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118023888-A-G

21687359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118023659-G-C

21687359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118023659-G-T

21687414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118023586-G-A

21687414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118023586-G-C

http://identifiers.org/hco/7/GRCh38#21687588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118023365-C-A

http://identifiers.org/hco/7/GRCh38#21687599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118023354-C-A

21687599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118023354-C-T

21687624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118023329-T-A

21687658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118023307-T-A

21687671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118023294-T-A

21687671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118023294-T-C

21687676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118023284-T-A

21687676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118023284-T-C

21687676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118023284-T-G

21688408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118023067-A-G

21688426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118023049-C-T

21688508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118022975-A-G

21688629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118022853-T-C

21688629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118022853-T-G

21688647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118022835-G-A

21688781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118022725-C-T

21688823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118022692-A-T

21688892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118022628-G-A

21688976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118022542-A-G

21689043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118022446-A-T

21689223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118022318-C-G

http://identifiers.org/hco/7/GRCh38#21689246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118022298-C-A

21689358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118022192-G-A

21689475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118022077-A-G

21689702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118021882-A-T

21690024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118021629-T-C

21690051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118021602-T-C

21690051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118021602-T-G

21690066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118021587-G-T

21690124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118021533-T-C

21690183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118021484-G-T

21690372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118021309-G-A

21690497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118021195-T-C

21690564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118021141-T-A

21690564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118021141-T-C

21690802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118020905-T-C

21690817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118020890-A-G

21690874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118020833-C-G

21690874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118020833-C-T

21696035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118017080-T-A

21696107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118017013-A-G

21696254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118016867-T-A

21696313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118016814-T-C

21696333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118016794-T-C

21696428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118016702-A-G

21696584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118016495-A-T

21696723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118016196-C-T

21696823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118015965-T-C

21696829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118015958-G-T

http://identifiers.org/hco/7/GRCh38#21696879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118015893-A-C

http://identifiers.org/hco/7/GRCh38#21696948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118015824-C-A

21696948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118015824-C-G

21697047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118015737-G-T

21697383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118015407-T-A

http://identifiers.org/hco/7/GRCh38#21697647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118015000-C-A

21697973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118014603-A-T

21698025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118014551-A-G

21698037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118014539-G-A

21698037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118014539-G-T

http://identifiers.org/hco/7/GRCh38#21698067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118014507-C-A

21698100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118014474-A-G

21698106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118014468-C-G

21698106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118014468-C-T

21698947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118014209-T-G

21698960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118014196-C-T

21699116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118014040-G-T

21699191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118013972-A-G

21699241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118013928-T-C

21699375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118013843-A-G

21699488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118013749-C-T

21699520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118013714-A-G

21699520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118013714-A-T

21699571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118013663-G-C

http://identifiers.org/hco/7/GRCh38#21699602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118013563-A-C

21699823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118013323-G-A

21702339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118011388-C-G

http://identifiers.org/hco/7/GRCh38#21702345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118011382-C-A

21702518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118011232-G-A

21702518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118011232-G-T

21702524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118011226-G-T

21702605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118011157-G-A

21702605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118011157-G-T

21702677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118011098-A-G

http://identifiers.org/hco/7/GRCh38#21702858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118010914-A-C

21702858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010914-A-G

21702892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010880-A-G

21702943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010834-G-T

21702948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010829-G-A

21703192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010573-C-T

21703238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010542-A-G

21703239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010541-C-T

21703275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010510-G-C

21703863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118010300-T-C

21703907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118010259-T-G

21703911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118010255-T-A

http://identifiers.org/hco/7/GRCh38#21703915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118010251-C-A

21703915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118010251-C-G

21703915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118010251-C-T

21703942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118010230-A-G

21704101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118010066-C-G

21704143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118010024-A-G

21704199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118009975-C-T

http://identifiers.org/hco/7/GRCh38#21704325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118009724-C-A

21704424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118009506-T-A

21704424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118009506-T-C

21704489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118009387-T-A

21704623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118009253-C-T

21704645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118009232-C-T

21704767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118009112-T-C

http://identifiers.org/hco/7/GRCh38#21704801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118009075-A-C

21705043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118008849-C-G

21705043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118008849-C-T

21705079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118008822-C-T

21705345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118007667-T-A

21705345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118007667-T-C

21705418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118007603-A-G

21705543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118007480-G-C

http://identifiers.org/hco/7/GRCh38#21705609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118007423-C-A

21705609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118007423-C-G

21705611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118007421-A-G

21705623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118007409-A-G

http://identifiers.org/hco/7/GRCh38#21705630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118007405-C-A

21705630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118007405-C-T

21705725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118007309-C-T

21705947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118006499-A-T

21706287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118006160-G-A

21706341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118006106-T-C

21706659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118005790-T-C

http://identifiers.org/hco/7/GRCh38#21706872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118005598-A-C

21707420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118005088-C-T

21707442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118005069-G-A

21707467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118005044-A-G

21707572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118004939-T-C

21707606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118004905-A-G

21707606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118004905-A-T

21708110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118004437-C-T

21708224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118004292-G-A

http://identifiers.org/hco/7/GRCh38#21709689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118003268-C-A

21709689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118003268-C-T

21709716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118003242-T-C

21709771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118003188-A-T

21710079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118003008-C-T

21710203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118002888-T-C

21710213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118002878-G-T

21710362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118002731-G-A

21710362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118002731-G-T

21710487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118002597-G-T

21710500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118002584-A-T

21710532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118002561-C-G

21710556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118002544-T-C

21710556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118002544-T-G

http://identifiers.org/hco/7/GRCh38#21710564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118002536-C-A

21710564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118002536-C-T

21710565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118002535-T-C

21710579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118002521-T-C

21710686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118002414-G-A

21710714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118002386-C-T

http://identifiers.org/hco/7/GRCh38#21710742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118002359-C-A

21710742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118002359-C-T

21710936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118001992-G-C

21711264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118001664-T-C

21711548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118000445-A-G

21711721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118000262-C-T

21711766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 118000217-C-T

21711805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 118000178-A-G

http://identifiers.org/hco/7/GRCh38#21711908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#118000067-C-A

21711908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118000067-C-T

21711937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 118000021-G-A

http://identifiers.org/hco/7/GRCh38#21711964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117999997-A-C

21711964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117999997-A-G

http://identifiers.org/hco/7/GRCh38#21712021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117999975-A-C

21712104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117999906-A-G

http://identifiers.org/hco/7/GRCh38#21712172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117999870-A-C

21712440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117999660-G-C

21713117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117999086-A-G

21713130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117999081-T-C

21713142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117999069-C-T

21713278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117998954-T-C

21713514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117998718-C-T

21713540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117998592-T-C

21713545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117998587-T-C

21713964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117998007-T-G

21713987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117997990-C-T

21714112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117997882-T-A

http://identifiers.org/hco/7/GRCh38#21714292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117997725-C-A

21714396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117997626-T-C

21714605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117997441-C-T

http://identifiers.org/hco/7/GRCh38#21714704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117997359-C-A

21714704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117997359-C-T

21714915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117997142-T-C

21714915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117997142-T-G

http://identifiers.org/hco/7/GRCh38#21715000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117997057-C-A

21715096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117996941-T-A

21715198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117996837-C-T

21715263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117996816-T-C

21715756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117996220-C-G

21715809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117996168-A-G

http://identifiers.org/hco/7/GRCh38#21715830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117996147-C-A

http://identifiers.org/hco/7/GRCh38#21715872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117996130-A-C

21715872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117996130-A-G

21715893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117996109-A-G

21715893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117996109-A-T

21715998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117996005-G-A

21715998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117996005-G-T

21716048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117995955-C-T

21716057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117995946-C-T

21716561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117995439-G-C

21716573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117995436-C-G

21716904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117994994-G-A

21716904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117994994-G-C

21716924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117994974-G-C

21717272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117994633-G-A

http://identifiers.org/hco/7/GRCh38#21717667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117994250-C-A

http://identifiers.org/hco/7/GRCh38#21717687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117994230-C-A

21717687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117994230-C-T

http://identifiers.org/hco/7/GRCh38#21717745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117994173-C-A

http://identifiers.org/hco/7/GRCh38#21717854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117994064-C-A

21717854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117994064-C-T

21717917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117994001-C-G

21717917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 117994001-C-T

21718032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117993841-G-T

21718253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117993546-A-G

21718386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117992981-G-C

http://identifiers.org/hco/7/GRCh38#21718435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117992934-A-C

http://identifiers.org/hco/7/GRCh38#21718703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117992760-A-C

21718804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117992684-G-C

21719423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117992081-C-G

21719423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117992081-C-T

21719425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117992079-G-A

21719444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117992068-A-G

21719447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117992065-C-T

21719448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117992064-A-G

21719489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117992026-T-C

21719505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117992010-T-A

21719516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991999-G-T

21719561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991955-A-G

21719705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991862-T-C

21719705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991862-T-G

21719919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991682-C-G

21719919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991682-C-T

21720476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991573-A-T

21720480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991569-G-T

21720528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991527-T-C

21720582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991462-A-G

21720582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991462-A-T

21720876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991161-A-G

21720898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991143-T-C

21720932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991119-G-A

21720932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991119-G-C

21720932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991119-G-T

21720947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991106-G-A

21720963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991099-A-G

http://identifiers.org/hco/7/GRCh38#21720996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117991070-C-A

21720996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117991070-C-T

21721203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117990927-C-T

21721311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117990844-A-T

21721417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117990760-T-C

21721658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117990584-T-C

21721658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117990584-T-G

21721715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117990529-C-G

21721774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117990474-G-T

21722255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117990030-T-C

21722298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117989987-G-A

21722355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117989933-C-T

21722533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117989780-C-T

21724092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117989528-A-G

21724176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117989448-C-T

21724191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117989433-T-A

21724360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117989250-G-A

21724363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117989247-C-G

21724363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117989247-C-T

21724366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117989244-C-T

21724450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117989109-A-G

21724515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117989042-G-C

21724574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988993-A-G

21724611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988963-A-G

21724612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988962-G-A

21724710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988906-G-A

21724723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988893-G-A

http://identifiers.org/hco/7/GRCh38#21724764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117988858-A-C

21724764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988858-A-G

21724764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988858-A-T

21724901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988768-T-C

http://identifiers.org/hco/7/GRCh38#21724921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117988748-C-A

http://identifiers.org/hco/7/GRCh38#21724922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117988747-C-A

21724922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988747-C-T

21724949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988737-C-G

21724949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988737-C-T

21725227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988539-C-T

http://identifiers.org/hco/7/GRCh38#21725354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117988388-C-A

21725494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988106-G-T

21725514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117988086-T-G

21725774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117987752-T-C

21725790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117987736-G-T

21725972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117987555-T-A

21725972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 117987555-T-C

21725993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117987534-G-A

21727517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117986942-T-C

21727521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117986938-T-C

21733626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117986552-C-T

21734099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117985784-T-C

21734105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117985776-A-G

http://identifiers.org/hco/7/GRCh38#21734231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117985679-A-C

21734231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117985679-A-G

21734336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117985581-T-C

21734343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117985574-A-G

21734443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117985488-T-A

21734473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117985453-T-C

21734559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117985367-A-G

21735299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117984421-C-G

21735299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117984421-C-T

21735316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117984405-T-C

21735413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117984307-G-A

21735413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117984307-G-T

21735431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117984289-C-T

21735432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117984288-C-T

21735458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117984267-C-G

21735498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117984246-G-A

21735498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117984246-G-T

21735556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117984190-T-A

21735556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117984190-T-C

21735556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117984190-T-G

http://identifiers.org/hco/7/GRCh38#21735673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117984092-C-A

21735689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117984076-A-G

21735689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117984076-A-T

21735699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 117984066-T-A

http://identifiers.org/hco/7/GRCh38#21735712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117984053-C-A

21735712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117984053-C-T

21735796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117983969-G-A

http://identifiers.org/hco/7/GRCh38#21735924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117983878-A-C

21735965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117983851-A-G

21735965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117983851-A-T

21736178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117983526-T-A

21736178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117983526-T-G

21737866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117983134-G-A

21737902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117983109-A-G

http://identifiers.org/hco/7/GRCh38#21738556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117982739-C-A

21738606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117982717-T-A

21738606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117982717-T-C

21738667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117982643-T-A

21738667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117982643-T-C

21738721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117982584-G-A

21738721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: stop gained
orthologous variants: 117982584-G-T

http://identifiers.org/hco/7/GRCh38#21738818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117982487-C-A

21739191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981816-G-C

21739191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981816-G-T

21739296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981699-T-C

21739334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981653-A-G

21739350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981632-C-T

21739409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981594-T-C

21739466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981537-G-A

21739466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981537-G-C

21739466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981537-G-T

http://identifiers.org/hco/7/GRCh38#21739467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117981536-A-C

21739467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981536-A-G

http://identifiers.org/hco/7/GRCh38#21739468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117981535-A-C

21739468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981535-A-G

21739468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981535-A-T

21739480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981527-A-T

21739499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981508-T-A

21739499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981508-T-G

21739507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981500-G-A

21739507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981500-G-C

21739507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981500-G-T

http://identifiers.org/hco/7/GRCh38#21739686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117981322-A-C

21739717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981268-G-A

21739717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981268-G-T

21739750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981234-G-A

21739750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981234-G-T

21739756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981220-T-G

21739852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117981035-A-G

21740044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117980843-T-C

21740088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117980801-C-T

21740132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117980758-C-T

21740182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117980714-A-G

21740215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117980676-T-G

21740328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117980571-C-T

21740369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117980517-G-A

http://identifiers.org/hco/7/GRCh38#21740519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117980369-C-A

21740519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117980369-C-G

21740519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117980369-C-T

21740590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117980316-T-G

21740624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117980294-T-C

21740627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117980291-A-G

21740700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117980228-T-G

http://identifiers.org/hco/7/GRCh38#21741124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117979810-A-C

21741149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979785-A-G

21741179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979756-G-A

21741179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979756-G-T

21741213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979735-A-G

21741559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979629-G-A

21741603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979586-T-C

21741611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979578-G-A

21741734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979452-T-G

21741761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979440-T-C

21741812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979387-A-G

http://identifiers.org/hco/7/GRCh38#21741821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117979378-C-A

21741821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979378-C-G

http://identifiers.org/hco/7/GRCh38#21741822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117979377-A-C

21741822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979377-A-G

21741822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979377-A-T

21741874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117979320-A-G

21742026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, missense_variant
orthologous variants: 117979165-G-C

21742085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 117979106-G-A

21742085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, missense_variant
orthologous variants: 117979106-G-C

21742085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, missense_variant
orthologous variants: 117979106-G-T

21742878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117978752-T-C

21743003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117978633-G-C

21743043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117978521-C-G

http://identifiers.org/hco/7/GRCh38#21743044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117978520-A-C

21743649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117977795-T-A

21743657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117977785-G-A

http://identifiers.org/hco/7/GRCh38#21743688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117977752-A-C

21743895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117977569-C-G

21743895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117977569-C-T

21743969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117977505-G-A

21744147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117977318-A-G

21744210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117977253-A-G

21744239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117976778-G-A

http://identifiers.org/hco/7/GRCh38#21744392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117976628-C-A

21744392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117976628-C-T

21744409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117976611-A-G

21744537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, missense_variant
orthologous variants: 117976483-G-A

21744537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, missense_variant
orthologous variants: 117976483-G-T

21744611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117976409-A-G

21744611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117976409-A-T

21744614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117976406-G-A

http://identifiers.org/hco/7/GRCh38#21744616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117976404-C-A

21744616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117976404-C-T

21744650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117976372-A-G

21744650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117976372-A-T

http://identifiers.org/hco/7/GRCh38#21744737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117976282-C-A

21744737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117976282-C-G

21744737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117976282-C-T

21744859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117976194-T-C

http://identifiers.org/hco/7/GRCh38#21744885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117976168-A-C

21744885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117976168-A-G

21744900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117976153-C-T

21744919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: coding_sequence_variant, missense_variant, undefined
orthologous variants: 117976134-T-C

21744968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 117976085-A-G

21745008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117976045-A-G

http://identifiers.org/hco/7/GRCh38#21745080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117975973-C-A

21745080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117975973-C-G

21745080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117975973-C-T

http://identifiers.org/hco/7/GRCh38#21745389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117975721-A-C

21745453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117975647-G-A

21745504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117975596-G-C

21745525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117975575-C-T

21745544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117975568-G-A

21745544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117975568-G-C

21746796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117974611-G-A

21746883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117974540-C-G

21746944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117974473-G-C

21747222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117974203-T-C

21748534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973935-G-A

21748534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973935-G-C

21748534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973935-G-T

21748713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117973751-A-G

http://identifiers.org/hco/7/GRCh38#21748773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117973397-C-A

21748773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973397-C-T

http://identifiers.org/hco/7/GRCh38#21748822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117973348-C-A

21748834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973342-G-A

21748834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973342-G-C

21748834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973342-G-T

21748839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973337-G-A

21748839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973337-G-C

21748839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973337-G-T

21748845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973331-G-A

http://identifiers.org/hco/7/GRCh38#21748853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117973323-C-A

21748891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973293-G-T

21749016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973177-G-A

21749143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973048-G-A

21749197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973024-A-G

21749218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117973002-T-C

21749418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117972794-G-A

21749567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117972694-C-T

http://identifiers.org/hco/7/GRCh38#21749568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117972693-C-A

21749568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117972693-C-T

21749609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117972663-A-G

http://identifiers.org/hco/7/GRCh38#21749614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117972658-C-A

http://identifiers.org/hco/7/GRCh38#21749618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117972654-C-A

21749618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117972654-C-G

21749643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 117972630-T-G

21749696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117972573-T-C

21749736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117972533-T-G

21749878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117972391-A-G

21750032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117972224-G-A

21750032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117972224-G-T

21750106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117971958-A-G

http://identifiers.org/hco/7/GRCh38#21750164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117971898-A-C

21750164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117971898-A-T

21750198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117971865-A-G

21750204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117971859-A-G

21750302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117971760-A-G

21750308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117971754-G-A

21750308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117971754-G-C

21750308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117971754-G-T

21750384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117971678-T-C

21750573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117971487-A-G

21750619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117971443-A-G

http://identifiers.org/hco/7/GRCh38#21750692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117971370-A-C

21750692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117971370-A-T

21750731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117971330-C-T

21750733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117971328-G-A

21751674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117971116-T-A

21751674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117971116-T-C

21753190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117970178-C-G

21753214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117970154-G-T

21753336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117970027-G-A

21753337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117970026-G-A

21753352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117970011-G-A

http://identifiers.org/hco/7/GRCh38#21753554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117969570-A-C

http://identifiers.org/hco/7/GRCh38#21753641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117969485-A-C

21754030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117968705-T-C

21754133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117968617-T-C

21754162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117968586-T-C

21754193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117968555-A-T

21754228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117968521-A-G

21754402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117968347-C-T

21754913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117968142-A-G

21755101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 117968001-A-G

21755504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117967638-A-G

21755506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117967636-G-C

21755545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117967595-A-T

21755632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117967510-A-G

21755646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117967496-T-G

21755858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117967279-T-G

http://identifiers.org/hco/7/GRCh38#21758573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117965799-A-C

http://identifiers.org/hco/7/GRCh38#21758685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117965711-A-C

http://identifiers.org/hco/7/GRCh38#21759241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117964373-A-C

21760126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117963508-G-A

21760229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117963406-A-G

21760329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117963319-C-G

21760337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117963315-G-A

http://identifiers.org/hco/7/GRCh38#21760441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117963212-C-A

21760522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962964-G-C

21760522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962964-G-T

21760549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962937-A-G

21760564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962912-G-T

http://identifiers.org/hco/7/GRCh38#21760786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117962675-A-C

21760786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962675-A-G

21760796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962666-G-A

21760805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962655-C-G

21760841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962622-A-G

21760863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962602-G-T

21761001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962478-G-T

21761022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962457-T-G

http://identifiers.org/hco/7/GRCh38#21761076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117962405-C-A

21761094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962388-G-A

21761094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962388-G-T

21761331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117962143-T-C

21765071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117959334-G-T

21765239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117959189-G-T

21765321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 117959131-A-T

http://identifiers.org/hco/7/GRCh38#21765339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#117959113-A-C

21765339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 117959113-A-G

21765339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 117959113-A-T

http://identifiers.org/hco/7/GRCh38#21765411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117959040-C-A

21765566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117958885-A-G

21765566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117958885-A-T

21765575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117958876-A-G

http://identifiers.org/hco/7/GRCh38#21765596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117958855-C-A

21765596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 117958855-C-T

http://identifiers.org/hco/7/GRCh38#21765605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117958846-C-A

21766134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117958666-T-C

21766196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117958627-G-A

21766286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117958561-T-A

21766485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117958374-A-G

http://identifiers.org/hco/7/GRCh38#21766693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117958204-C-A

21766704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117958192-G-T

http://identifiers.org/hco/7/GRCh38#21766918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117958014-C-A

21766918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117958014-C-T

http://identifiers.org/hco/7/GRCh38#21766948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117957984-C-A

http://identifiers.org/hco/7/GRCh38#21766955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117957966-A-C

21767376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117957477-C-G

21767424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 117957442-C-T

http://identifiers.org/hco/7/GRCh38#21767588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#117957291-A-C

21767650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 117957230-C-T

21768274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117956623-C-T

21768275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117956622-G-A

21768407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117956491-T-C

21768464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117956435-G-C

http://identifiers.org/hco/7/GRCh38#21768827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117956089-A-C

21768862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117956055-T-C

21769287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117955173-G-T

21770696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117954397-G-A

21770729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117954374-A-G

21770929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117954195-T-A

21771091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117954049-T-G

21771183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117953945-C-T

21771245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117953911-T-A

21771269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117953887-A-G

21771372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117953799-A-G

21771880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117953336-G-A

21771880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117953336-G-T

21772582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117952678-C-T

21772616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117952644-G-A

http://identifiers.org/hco/7/GRCh38#21772807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117952463-A-C

21772807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117952463-A-G

21772907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117952379-C-T

21773104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117952182-T-C

21773168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117952064-G-A

21773500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117951573-T-G

21773547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117951514-T-A

21773938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117951114-T-A

21773938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117951114-T-C

http://identifiers.org/hco/7/GRCh38#21773979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117951073-C-A

21773979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117951073-C-G

21774282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117949150-C-G

21774293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117949139-A-G

21774392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117949033-G-A

21774408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117949017-G-A

21774525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117948887-G-A

21776016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117948501-T-C

21776056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117948468-G-C

21776183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117948342-C-T

21777668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117947967-T-C

21777896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117947765-C-T

21778098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117947620-T-C

21778583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117947193-C-T

21778752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117947035-T-C

21778779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946995-A-G

21778779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946995-A-T

21778814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946957-A-G

21778820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946951-A-G

21778849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946922-G-A

21778849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946922-G-T

http://identifiers.org/hco/7/GRCh38#21778859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117946913-A-C

21778859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946913-A-G

http://identifiers.org/hco/7/GRCh38#21778873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117946899-C-A

21778873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946899-C-G

21778873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946899-C-T

21778875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946897-T-C

21778875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946897-T-G

http://identifiers.org/hco/7/GRCh38#21778881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117946891-C-A

21778881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946891-C-T

21778896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946876-G-A

21778896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946876-G-T

21779021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117946765-G-T

21779054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117946732-A-G

21779084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117946702-G-A

21779084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117946702-G-T

21779289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946497-C-G

http://identifiers.org/hco/7/GRCh38#21779482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117946305-C-A

21779533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946254-G-C

21779578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946205-A-T

21779659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117946124-A-G

21779958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117945869-T-C

21780008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117945822-A-G

21780064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117945770-G-C

21780064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117945770-G-T

21780223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117945636-G-T

21780232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117945627-C-T

21780485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117945522-A-G

21780533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117945462-C-T

21780783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117945212-G-A

21781944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117944854-T-G

21781952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117944845-G-T

21782177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117944463-C-T

21782285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117944359-C-T

21782302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117944342-C-G

21782381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117944265-T-C

21782558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117944116-G-T

21783017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117943979-T-G

http://identifiers.org/hco/7/GRCh38#21783081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117943919-A-C

21783180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117943815-G-A

21783220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117943775-A-T

http://identifiers.org/hco/7/GRCh38#21783504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117943491-C-A

21783668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117943349-G-T

21783898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117943170-T-C

21783947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117943124-T-C

21783947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117943124-T-G

21783978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117942739-G-A

http://identifiers.org/hco/7/GRCh38#21784015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117942701-A-C

21784065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117942651-G-C

21784175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117942514-G-C

21784354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117942376-A-G

21784460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: stop gained
orthologous variants: 117942271-C-T

21784550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117942182-A-G

21784558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117942174-G-A

21784558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117942174-G-C

21784585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117942154-T-C

21784585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117942154-T-G

http://identifiers.org/hco/7/GRCh38#21784652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117942089-A-C

21784652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117942089-A-T

21784785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117941868-A-G

21784925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117941628-G-A

21785020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117941538-C-G

21785034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117941524-C-G

21785092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117941474-G-T

21785223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117941342-A-G

21785373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117941205-A-G

21785849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117940216-T-G

21785986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117940164-T-C

21786050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117940102-C-G

21786270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117939884-T-C

21786570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117939638-T-A

21786669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117939558-G-C

21786779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117939446-G-A

21786779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117939446-G-C

21786820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117939405-C-T

21786915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117939302-A-G

21786950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117939263-T-C

21786961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117939252-G-A

21787383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117938825-A-G

21787392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117938816-G-A

21787470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117938738-G-A

21787518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117938690-C-G

21787518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: stop gained
orthologous variants: 117938690-C-T

21787591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 117938613-T-C

21787975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117937214-G-C

21788117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117937098-T-G

21788197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117937020-T-C

21788283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117936934-T-C

21788283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117936934-T-G

21788314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117936905-G-A

21788339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117936880-G-A

http://identifiers.org/hco/7/GRCh38#21788371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117936848-C-A

21788394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117936824-A-G

21788890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117936361-T-A

21789188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117936216-G-A

21789192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117936212-G-C

http://identifiers.org/hco/7/GRCh38#21789201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117936203-C-A

21789201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117936203-C-T

21789322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117936068-G-A

21789322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117936068-G-T

http://identifiers.org/hco/7/GRCh38#21789423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117935969-C-A

21789664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117935757-C-T

21789666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117935755-C-T

21790696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117935216-G-A

21791024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117934891-G-T

21791139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117934778-C-T

21791200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117934724-T-G

21791290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117934630-C-T

21791294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117934626-C-G

21791492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117934430-T-C

21791595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117934326-T-C

21791706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117934239-C-G

21799999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117931281-A-G

21800057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117931237-A-G

21800124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117931173-G-C

21800278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117931038-C-T

21800544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930816-A-G

21800677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930731-G-C

21800677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930731-G-T

21800709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930727-G-C

21800710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930726-A-T

21800727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930709-G-C

21800817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930707-G-A

21800925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930597-A-G

21801013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930513-G-T

21801025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930505-A-G

21801059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930478-T-A

21801059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930478-T-C

21801075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930462-A-G

21801295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930248-A-G

21801297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930246-A-G

21801297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930246-A-T

21801351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930196-T-C

21801368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117930179-T-C

21801785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117928966-T-G

21801894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117928862-A-G

21801962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117928799-A-T

21801999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117928755-A-T

21802287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117928510-A-G

21802303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117928494-C-T

http://identifiers.org/hco/7/GRCh38#21803145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117927811-A-C

http://identifiers.org/hco/7/GRCh38#21805763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117926827-A-C

21805770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117926820-T-C

21805786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117926804-A-G

21806233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117926360-A-G

21806263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117926331-G-A

21806398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117926207-G-C

21806508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117926143-C-T

21806541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117926105-G-A

21806548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117926098-T-C

http://identifiers.org/hco/7/GRCh38#21806605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117926038-C-A

21806792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117925846-T-C

21806915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117925711-C-G

21806932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117925694-A-G

21806969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117925657-T-C

http://identifiers.org/hco/7/GRCh38#21807204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117925433-A-C

21807515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117925247-A-G

21807566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117925209-G-A

21807597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117925177-G-A

21807649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117925126-A-G

21807682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117925089-A-T

http://identifiers.org/hco/7/GRCh38#21807739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117925032-C-A

21807739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117925032-C-T

http://identifiers.org/hco/7/GRCh38#21807767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117925005-C-A

21807767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117925005-C-T

21807836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117924931-G-A

21807836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117924931-G-T

21807856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117924911-A-G

21807856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117924911-A-T

21807874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117924893-T-C

http://identifiers.org/hco/7/GRCh38#21807951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117924816-C-A

21807951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117924816-C-T

21807969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117924798-G-A

21807969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117924798-G-T

21807981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117924786-G-A

http://identifiers.org/hco/7/GRCh38#21808057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117924710-C-A

21808057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 117924710-C-G

21808057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 117924710-C-T

21808138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117924628-G-A

21810023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117924488-A-T

21810714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117920591-A-G

21810729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117920577-G-A

21810773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117920528-A-G

21810916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117920391-A-G

http://identifiers.org/hco/7/GRCh38#21811066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117920246-C-A

21811777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117919859-T-C

21812046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117919679-A-G

21812312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117919454-T-C

21812844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117919239-G-A

21813057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117919035-G-A

http://identifiers.org/hco/7/GRCh38#21816369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117918785-C-A

21816369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117918785-C-G

21816369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117918785-C-T

21816429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117918717-A-G

21816515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117918631-G-A

21816691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 117918455-G-A

21817248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117917971-T-C

21818067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117916510-G-A

21818067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117916510-G-T

21818074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117916503-G-T

http://identifiers.org/hco/7/GRCh38#21818154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117916418-A-C

21818154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117916418-A-G

21818164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117916408-A-G

21818361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117916201-A-T

21818413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117916146-G-T

21818428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117916129-G-A

21818428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117916129-G-T

21818589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117915987-T-C

21818638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117915941-A-G

21818658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117915920-G-C

21818771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117915758-C-T

21818869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117915628-C-T

http://identifiers.org/hco/7/GRCh38#21818882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117915617-A-C

21819154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117915075-C-G

21819154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117915075-C-T

21819243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117914995-G-A

21819312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117914934-G-A

21819657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117914591-G-A

21819808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117914436-A-G

21819808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117914436-A-T

21823703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117911490-G-A

21823909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117911321-T-C

21824031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117911202-G-A

21824031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117911202-G-T

http://identifiers.org/hco/7/GRCh38#21826521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117908356-C-A

21826521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117908356-C-G

21826521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117908356-C-T

http://identifiers.org/hco/7/GRCh38#21826553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117908301-C-A

21826711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117907987-C-G

21826827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117907869-C-T

21826866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117907832-T-G

21826878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117907777-T-C

21827559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117907116-A-G

21828660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117906301-G-T

21828915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117906017-T-C

21828942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117905986-T-C

21829371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117905674-T-C

http://identifiers.org/hco/7/GRCh38#21829505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117905565-A-C

21829560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117905510-C-T

21829658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117905412-T-G

21829746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117905348-T-C

21829826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117903377-C-G

21829894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117903316-G-T

21830035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117903177-T-C

21830551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117902707-A-G

21830717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117902551-T-A

http://identifiers.org/hco/7/GRCh38#21830725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117902543-C-A

21830755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117902512-A-G

21830771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117902496-C-G

21831047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117902291-G-C

21831291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117902089-C-T

21831325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117902056-T-C

21831556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117901824-A-G

21831691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117901414-T-A

21831725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117901380-G-A

21831725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117901380-G-C

21839597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117899383-T-A

21839597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117899383-T-G

21839764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117899231-G-A

21839764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117899231-G-T

21839830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117899170-T-A

21839962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117899054-T-A

21840094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117898938-G-C

21840143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117898890-T-C

21840499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117898334-C-T

21841348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117897799-T-G

21842569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117897594-T-C

21842647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117897516-C-G

21842686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117897477-C-G

21842686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: 117897477-C-T

http://identifiers.org/hco/7/GRCh38#21842716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117897447-A-C

21842716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117897447-A-G

21842775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117897388-A-G

21851746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117895426-T-C

21851750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117895422-T-A

21851781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117895387-G-A

21851823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117895350-T-G

21852030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117895149-G-A

21852145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117895114-C-T

21852278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117895109-G-T

http://identifiers.org/hco/7/GRCh38#21852393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117895075-C-A

21852393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117895075-C-G

21852393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117895075-C-T

http://identifiers.org/hco/7/GRCh38#21852434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117895055-A-C

http://identifiers.org/hco/7/GRCh38#21852488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117895010-A-C

21852518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117894980-G-A

21852596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117894902-G-A

21852596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117894902-G-C

21852639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 117894859-G-C

21852700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117894141-T-C

http://identifiers.org/hco/7/GRCh38#21852710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117894131-C-A

21852710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117894131-C-G

21852778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117894048-G-A

21852868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117893977-T-G

21853053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117893828-G-A

21853172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117893710-T-C

21853174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117893708-T-A

21853376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117893515-G-A

21853558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117893366-C-T

21853659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117893260-T-A

21853783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117893127-G-A

21854014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117892891-G-A

21854094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117892805-C-G

21854154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117892735-A-G

21854190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117892693-G-A

21854190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117892693-G-C

21854190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117892693-G-T

21854304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117892203-T-A

21854378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117892129-G-A

21854378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117892129-G-T

21854480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117892027-A-G

21854481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117892026-T-C

21854481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117892026-T-G

http://identifiers.org/hco/7/GRCh38#21854499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117892007-C-A

21854499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117892007-C-G

http://identifiers.org/hco/7/GRCh38#21854521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117891980-A-C

21854521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117891980-A-G

21860220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117887284-T-A

http://identifiers.org/hco/7/GRCh38#21860254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117887247-A-C

21860254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117887247-A-G

21860254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117887247-A-T

21860407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117887128-A-G

http://identifiers.org/hco/7/GRCh38#21860436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117887097-A-C

21860438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117887095-T-G

21860652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117886891-A-G

21861152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117886584-G-A

21861177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117886559-A-T

21861212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117886526-A-G

21861708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117886081-G-A

21861708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117886081-G-T

21861724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117886041-T-C

http://identifiers.org/hco/7/GRCh38#21861744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117886021-C-A

21861744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117886021-C-G

21861744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117886021-C-T

21861760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117886005-A-G

http://identifiers.org/hco/7/GRCh38#21861774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117885991-C-A

21861885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117885884-G-A

21861885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117885884-G-C

21862035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117885734-A-G

21862129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117885653-T-A

21862141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117885641-G-A

21862141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117885641-G-T

21862224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117885585-T-A

21862296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117885549-A-G

21862296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117885549-A-T

21862579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117885295-A-G

21862600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117885274-T-C

21862631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117885243-T-C

21864451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117884841-A-G

http://identifiers.org/hco/7/GRCh38#21864492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117884802-C-A

21864492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117884802-C-T

21864500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117884794-C-T

http://identifiers.org/hco/7/GRCh38#21864681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117884614-A-C

21864707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117884586-A-G

21864718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117884575-G-A

21864718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117884575-G-T

http://identifiers.org/hco/7/GRCh38#21864769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117884529-C-A

21865067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117884268-T-G

http://identifiers.org/hco/7/GRCh38#21866302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117880852-C-A

21866302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880852-C-T

http://identifiers.org/hco/7/GRCh38#21866348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117880804-A-C

21866348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880804-A-G

21866348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880804-A-T

21866436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880755-C-T

21866459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880715-T-A

21866459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880715-T-C

21866485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: stop gained
orthologous variants: 117880689-G-T

21866504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117880670-A-G

21866620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117880554-C-G

21866620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117880554-C-T

21866629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117880545-G-A

21866629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117880545-G-C

http://identifiers.org/hco/7/GRCh38#21866638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117880536-C-A

21866638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117880536-C-T

21866650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117880524-A-T

21866672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880503-G-T

http://identifiers.org/hco/7/GRCh38#21866697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117880478-A-C

21866732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880447-G-A

21866777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880441-T-C

http://identifiers.org/hco/7/GRCh38#21866811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117880407-C-A

21866811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880407-C-T

21866823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880395-G-A

21866880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880333-A-G

21866911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880308-G-T

21866919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880300-T-C

21867039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880198-T-C

21867176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880062-C-G

http://identifiers.org/hco/7/GRCh38#21867244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117880000-C-A

21867244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117880000-C-G

21867322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879918-C-T

21867334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879905-T-G

21867358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879881-A-G

21867378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879862-T-G

21867565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879669-T-G

http://identifiers.org/hco/7/GRCh38#21867728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117879513-C-A

21867728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879513-C-T

21867730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879511-A-G

21867746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879496-T-A

21867746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879496-T-C

21867746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879496-T-G

21867896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: stop gained
orthologous variants: 117879303-G-T

21867911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117879288-G-A

21867911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117879288-G-T

http://identifiers.org/hco/7/GRCh38#21867946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117879253-C-A

21868019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879180-G-A

21868019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879180-G-C

21868019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879180-G-T

21868022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879177-G-A

21868027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879172-G-A

21868027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879172-G-C

21868027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879172-G-T

21868051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879156-T-A

21868051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879156-T-C

21868051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879156-T-G

21868056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879151-T-C

21868057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879150-T-A

21868057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879150-T-C

21868057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879150-T-G

21868110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117879101-T-C

21868354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 117878857-C-G

21868355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, undefined
orthologous variants: 117878856-T-C

http://identifiers.org/hco/7/GRCh38#21868397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117878816-C-A

21868548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117878669-G-T

21868656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117878562-A-G

21868670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117878546-G-C

http://identifiers.org/hco/7/GRCh38#21868721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117878495-C-A

21868721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117878495-C-G

21868779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117878447-A-G

21868820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117878412-T-C

21868821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117878411-C-G

21868825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117878407-C-T

21868947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117878283-G-A

21868948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117878282-C-T

21868999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 117878231-T-A

21868999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 117878231-T-C

21869001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117878229-A-G

21869040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117878189-G-A

21869105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117878126-G-T

http://identifiers.org/hco/7/GRCh38#21869123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117878118-C-A

21870468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117877502-G-C

21870485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117877476-G-C

21870528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117877434-G-A

21870667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117877298-T-C

21870747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117877232-T-C

21870753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117877226-G-A

21870766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117877213-T-C

http://identifiers.org/hco/7/GRCh38#21870783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117877196-A-C

http://identifiers.org/hco/7/GRCh38#21870852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117877148-C-A

21871055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117876940-T-C

21871124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117876872-C-T

21871205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117876802-A-G

21871205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117876802-A-T

http://identifiers.org/hco/7/GRCh38#21871495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117876659-C-A

21871495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117876659-C-T

21871909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117876393-T-A

21872178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117876249-T-C

21872179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117876248-T-C

21872205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117876221-A-G

21872590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117875729-G-A

21872916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117875362-T-C

21873292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: stop gained
orthologous variants: 117874960-A-T

21873454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117874798-A-G

http://identifiers.org/hco/7/GRCh38#21873482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117874770-C-A

21873568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117874685-G-A

21873568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117874685-G-C

21873568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117874685-G-T

21875134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117873215-T-C

21875284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117873146-A-T

http://identifiers.org/hco/7/GRCh38#21877425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117870073-C-A

21878215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117869196-G-A

21878620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117868581-T-C

21878804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117868417-T-C

21878827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117868394-C-T

21879144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117868128-G-A

21879144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117868128-G-T

21879165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117868107-A-T

http://identifiers.org/hco/7/GRCh38#21880159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117867713-A-C

21880159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117867713-A-G

21880382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117867494-A-G

21880382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117867494-A-T

http://identifiers.org/hco/7/GRCh38#21880522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117867293-C-A

21880522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117867293-C-T

21880611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117867116-A-G

http://identifiers.org/hco/7/GRCh38#21880639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117867089-C-A

21880639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117867089-C-G

21880656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117867072-A-G

21880656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117867072-A-T

21880662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117867066-T-A

21880662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117867066-T-G

21880676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117867052-C-T

21880756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117866972-C-G

21880756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117866972-C-T

21880852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117866876-T-G

21880861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117866867-G-A

21880888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117866840-T-C

http://identifiers.org/hco/7/GRCh38#21880891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117866837-A-C

21880891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 117866837-A-G

21880951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117866778-G-C

21880951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117866778-G-T

21880968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117866761-A-G

http://identifiers.org/hco/7/GRCh38#21880970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117866759-C-A

21880970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117866759-C-G

21880970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117866759-C-T

21880995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117866734-T-C

21881018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117866711-G-A

21881018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117866711-G-T

21881043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117866688-A-T

21881552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117866209-C-G

21881705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117866079-T-C

21881748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117866038-T-C

21881748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117866038-T-G

21881809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117865977-A-T

21881815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117865971-C-T

21882079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117865494-A-G

21882080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117865493-T-A

http://identifiers.org/hco/7/GRCh38#21882096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117865477-A-C

21882096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117865477-A-G

21882105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117865468-A-G

21882153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117865421-G-C

21882266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117865322-G-C

21882341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117865254-A-T

21882407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117865175-G-T

21883116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117863681-T-C

21884059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117859437-T-C

21884059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117859437-T-G

http://identifiers.org/hco/7/GRCh38#21884094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117859403-A-C

http://identifiers.org/hco/7/GRCh38#21884146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117859352-C-A

21884146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117859352-C-G

http://identifiers.org/hco/7/GRCh38#21884152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117859346-C-A

21884152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117859346-C-T

21884197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117859302-A-G

http://identifiers.org/hco/7/GRCh38#21884201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117859298-C-A

21884201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117859298-C-T

21884222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117859276-G-A

21884243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117859256-G-A

21884243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117859256-G-T

21884378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117858716-G-C

21884378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117858716-G-T

21884425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858669-A-G

21884425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858669-A-T

http://identifiers.org/hco/7/GRCh38#21884446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117858660-C-A

21884446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858660-C-T

21884459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858647-A-G

http://identifiers.org/hco/7/GRCh38#21884468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117858638-A-C

21884468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858638-A-G

21884468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858638-A-T

21884494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858609-G-A

21884494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858609-G-T

21884636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858523-A-T

21884739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858456-G-A

21884802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858400-G-A

http://identifiers.org/hco/7/GRCh38#21884833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117858370-C-A

21884904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858327-C-T

21884920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858312-A-G

21884995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858239-C-T

21884996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858238-C-T

21885033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858208-G-A

21885129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117858127-G-T

21885230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117857988-T-A

21885232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117857986-A-T

http://identifiers.org/hco/7/GRCh38#21885818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117857325-C-A

21885818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117857325-C-G

21885878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117857280-C-T

21885962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117857198-G-T

21886404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117856623-G-A

21886480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117856537-A-G

21886736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117856284-G-A

21886836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117856185-A-T

21887128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117855915-C-T

21887133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117855910-T-C

21887141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117855893-C-G

21887141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117855893-C-T

21887173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117855863-G-T

21887537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117855526-G-A

21887543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117855520-G-A

http://identifiers.org/hco/7/GRCh38#21887547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117855516-C-A

21887547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117855516-C-G

21887644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117855420-C-T

http://identifiers.org/hco/7/GRCh38#21887680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117855385-C-A

21887878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117854785-G-A

21887878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117854785-G-C

21887909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117854740-T-C

21887993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117854641-C-T

21888186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117854473-C-T

21888216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117854438-A-G

http://identifiers.org/hco/7/GRCh38#21888224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117854431-A-C

21888224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117854431-A-G

http://identifiers.org/hco/7/GRCh38#21888364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117854298-A-C

21890818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117852333-G-A

21890860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117852291-A-G

http://identifiers.org/hco/7/GRCh38#21891022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117852136-C-A

21891026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117852131-G-T

21891260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117851926-C-T

21891417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117851779-G-A

21891478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117851730-T-C

21891567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117851651-G-A

21891577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117851642-C-G

21891644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117851583-T-C

21891740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117851493-T-C

21891967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117851023-C-T

http://identifiers.org/hco/7/GRCh38#21892055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117850937-A-C

21892242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117850777-G-A

21892375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron variant
orthologous variants: 117850695-T-G

21892425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 117850647-A-G

21892461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense variant
orthologous variants: 117850611-G-A

http://identifiers.org/hco/7/GRCh38#21892729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117850363-A-C

21892729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117850363-A-G

21892769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117850320-T-G

21892801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117850283-T-C

21892931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117850182-G-A

21892975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117850147-T-C

21892994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117850128-T-G

21893025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117850098-T-C

21893126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117849995-A-G

http://identifiers.org/hco/7/GRCh38#21894087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117848237-C-A

21894212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117848136-G-T

21894219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117848128-T-C

21894483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117847952-G-A

21894483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117847952-G-T

21894638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117847458-G-A

21894638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117847458-G-C

21894680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117847416-G-A

21894764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117847332-G-A

21894856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117847234-A-G

21894856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117847234-A-T

21895009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117847085-C-T

21895010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117847084-C-T

21895032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117847064-T-C

21895461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117846671-G-T

21899233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117844391-T-A

21899233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117844391-T-C

http://identifiers.org/hco/7/GRCh38#21899234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117844390-C-A

21899234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117844390-C-T

http://identifiers.org/hco/7/GRCh38#21899246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117844378-C-A

21899246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117844378-C-T

21899263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117844357-C-T

http://identifiers.org/hco/7/GRCh38#21899317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117844316-C-A

21899317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117844316-C-T

21899577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117844073-A-G

21899675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117844011-G-A

21899822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843874-C-G

http://identifiers.org/hco/7/GRCh38#21899884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117843841-C-A

21899884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843841-C-G

21899884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843841-C-T

21899891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843834-G-T

21899943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843801-A-T

21900042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117843701-G-C

21900056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117843687-A-G

21900105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117843638-G-A

21900105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117843638-G-C

21900112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117843631-T-A

http://identifiers.org/hco/7/GRCh38#21900173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117843578-C-A

21900210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843555-C-G

21900210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843555-C-T

21900256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843533-T-A

21900264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843519-A-T

http://identifiers.org/hco/7/GRCh38#21900299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117843484-A-C

21900299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843484-A-G

21900302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843481-C-T

http://identifiers.org/hco/7/GRCh38#21900888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117842455-A-C

http://identifiers.org/hco/7/GRCh38#21900898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117842445-A-C

21901076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842287-C-G

21901076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842287-C-T

21901094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842269-C-G

21901129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842234-T-C

21901138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842225-C-T

21901228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842135-G-A

21901228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842135-G-C

21901265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117842087-G-C

21901296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117842057-A-G

21901401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841991-A-G

http://identifiers.org/hco/7/GRCh38#21901423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117841969-C-A

21901423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841969-C-G

http://identifiers.org/hco/7/GRCh38#21901443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117841966-C-A

21901443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841966-C-G

21901443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841966-C-T

http://identifiers.org/hco/7/GRCh38#21901484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117841941-A-C

21901484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841941-A-G

21901484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841941-A-T

http://identifiers.org/hco/7/GRCh38#21901680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117841831-C-A

21901692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841822-T-A

21901692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841822-T-C

http://identifiers.org/hco/7/GRCh38#21901775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117841744-A-C

21901775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2942
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841744-A-T