http://identifiers.org/hco/1/GRCh38#6424823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152236798-C-A

6424823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5 prime UTR variant
orthologous variants: 152236798-C-G

6424823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5 prime UTR variant
orthologous variants: 152236798-C-T

6424868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5 prime UTR variant
orthologous variants: 152236752-A-G

6424875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5 prime UTR variant
orthologous variants: 152236745-G-A

6424875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5 prime UTR variant
orthologous variants: 152236745-G-T

6424933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5 prime UTR variant
orthologous variants: 152236685-G-A

6424933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5 prime UTR variant
orthologous variants: 152236685-G-T

6424950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 152236668-G-A

6424950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 152236668-G-T

6425070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152236548-C-G

6425070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152236548-C-T

6425294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152236354-G-A

6425294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152236354-G-C

6425294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152236354-G-T

http://identifiers.org/hco/1/GRCh38#6425310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152236338-C-A

6425310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152236338-C-T

6425450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152236199-T-C

6425450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152236199-T-G

http://identifiers.org/hco/1/GRCh38#6425547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152236116-A-C

6425609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152236042-G-C

6425824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152235834-C-G

6425829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152235829-G-C

6426097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152235592-G-A

6426517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152235003-C-T

http://identifiers.org/hco/1/GRCh38#6426542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152234981-A-C

6426563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152234960-G-A

6426857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152234698-T-C

6427190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152234451-G-T

6427326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152234328-T-C

6427351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152234303-C-T

http://identifiers.org/hco/1/GRCh38#6427590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152234106-C-A

6427590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152234106-C-G

6427638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152234041-G-T

6427665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152234025-T-C

6428208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152233524-C-T

6428283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152233450-G-A

6428311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152233422-G-A

6428319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152233414-G-A

6428379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152233354-G-A

6428382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152233351-T-A

6428382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152233351-T-C

6428384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152233349-C-G

6428388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152233345-T-G

6428401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152233332-T-A

6428447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152233282-C-G

6428449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152233280-G-A

6428794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152232398-G-T

6429070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152232148-G-C

6429088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152232133-A-G

6429210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152232011-G-C

6429304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152231954-C-T

6429471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152231515-C-T

6429644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152231345-C-T

6429707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152231284-A-G

6429781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152231212-T-C

6429792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152231201-G-T

http://identifiers.org/hco/1/GRCh38#6429797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152231196-C-A

6429799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152231194-T-C

6429936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152231071-G-A

6429962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152231045-G-A

6429962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152231045-G-T

6430026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152230981-T-C

6430411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152230642-G-C

6430512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152230533-G-T

6435263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152228938-G-T

http://identifiers.org/hco/1/GRCh38#6437281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152226362-C-A

6437346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152226300-A-G

6437412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152226226-C-T

6437430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152226208-G-A

6437430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152226208-G-C

6437463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152226157-T-C

6437492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152226128-C-T

http://identifiers.org/hco/1/GRCh38#6437564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152226068-C-A

6437564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152226068-C-T

6437570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152226062-G-T

6437579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152226052-G-A

6437579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152226052-G-T

6437659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152225601-T-C

6437724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152225539-G-T

6437744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152225507-A-G

6437799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225455-G-A

6437799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225455-G-T

6437806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225448-A-G

6437821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225433-G-A

6437848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225426-G-T

6437893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225392-G-T

6438084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225220-G-A

http://identifiers.org/hco/1/GRCh38#6438141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152225157-A-C

6438141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225157-A-G

6438145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225153-G-A

6438145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225153-G-C

6438191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225139-G-C

6438230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225100-G-A

6438256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152225075-A-G

6438511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152224985-T-C

6439864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152224028-C-T

6439887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152224005-T-C

6440053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223853-G-A

6440053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223853-G-T

http://identifiers.org/hco/1/GRCh38#6440141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152223790-C-A

http://identifiers.org/hco/1/GRCh38#6440177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152223753-A-C

6440177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223753-A-T

6440248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 152223686-C-T

6440402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 152223532-G-A

6440402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 152223532-G-C

6440402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 152223532-G-T

6440427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152223507-T-A

6440427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152223507-T-C

6440529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152223446-G-A

6440529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152223446-G-C

6440529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152223446-G-T

6440542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223433-G-A

6440542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223433-G-C

6440542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223433-G-T

http://identifiers.org/hco/1/GRCh38#6440605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152223393-C-A

6440605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223393-C-G

6440605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223393-C-T

http://identifiers.org/hco/1/GRCh38#6440607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152223391-C-A

6440607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223391-C-G

6440607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152223391-C-T

6440729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152223270-T-A

6440729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152223270-T-C

6440767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152223232-G-A

6440767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152223232-G-T

6440819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152223180-G-A

6440819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152223180-G-T

http://identifiers.org/hco/1/GRCh38#6440870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152223078-C-A

6440870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152223078-C-T

6440919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152223031-T-C

6440943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152223007-A-G

6440970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152222980-G-A

6441079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152222871-G-T

6441157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152222792-C-G

6441157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152222792-C-T

6441160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152222789-A-G

6441556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152221928-T-C

6441649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152221834-G-T

6443220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152221368-T-A

6443220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152221368-T-C

6443401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152221207-C-T

6443498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152221102-G-A

6444021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152220583-C-G

6444122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152220499-T-C

6444125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152220496-G-A

6444125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152220496-G-C

6444125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152220496-G-T

6444147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152220457-G-A

6444197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152220380-A-G

6444342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152220251-T-C

6444350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152220243-A-G

http://identifiers.org/hco/1/GRCh38#6444388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152220211-C-A

6444388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152220211-C-T

6444497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 152220113-T-A

6444517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 152220093-G-A

6444547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 152220063-G-A

6444547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 152220063-G-T

6444610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 152220000-A-G

http://identifiers.org/hco/1/GRCh38#6444616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152219994-A-C

6444616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 152219994-A-G

6444619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 152219991-C-T

6444687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152219923-G-A

6444687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152219923-G-T

6444755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152219860-C-T

http://identifiers.org/hco/1/GRCh38#6444810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152219830-A-C

6444881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219789-A-T

6445027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152219647-G-A

6445094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152219583-T-C

6445094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152219583-T-G

6445112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152219543-C-T

6445141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152219493-C-T

6445163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219468-A-G

6445270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219225-C-T

6445271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219224-G-A

6445318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152219176-C-T

6445391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152219123-C-G

6445419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152219089-A-T

6445455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152219052-G-A

6445455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152219052-G-T

6445610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152218948-G-A

6445610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152218948-G-T

6445624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152218939-T-C

http://identifiers.org/hco/1/GRCh38#6445760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152218800-C-A

6445760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 152218800-C-T

http://identifiers.org/hco/1/GRCh38#6445764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152218796-A-C

6445764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 152218796-A-G

6445944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152218603-C-T

http://identifiers.org/hco/1/GRCh38#6446026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152218525-C-A

6446039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218513-T-A

6446039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152218513-T-G

6446077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152218475-G-A

6446077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152218475-G-T

6446554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152217631-G-C

6446554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152217631-G-T

6446835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152217397-A-T

http://identifiers.org/hco/1/GRCh38#6446850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152217385-C-A

6446885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152217351-A-G

6446885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152217351-A-T

6446888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152217348-G-A

http://identifiers.org/hco/1/GRCh38#6446907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152217331-C-A

6446907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152217331-C-G

6446907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152217331-C-T

6446922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152217316-G-T

6447031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152217210-A-G

http://identifiers.org/hco/1/GRCh38#6447043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152217200-C-A

6447061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152217178-C-T

http://identifiers.org/hco/1/GRCh38#6447079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152217160-C-A

6447079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152217160-C-T

6447353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 152216997-G-A

6447353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 152216997-G-T

6447517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152216834-G-T

6447930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152216433-G-A

6447930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152216433-G-T

6447933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152216430-T-C

6448022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152216340-G-A

6448022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152216340-G-T

6448149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152216218-T-C

6448149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152216218-T-G

6448164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152216202-A-G

6448291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152216075-T-C

6448377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152215990-T-C

http://identifiers.org/hco/1/GRCh38#6448509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215871-A-C

http://identifiers.org/hco/1/GRCh38#6448538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215841-C-A

6448538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 152215841-C-T

6448569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 152215812-G-A

6448569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 152215812-G-C

6448569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 152215812-G-T

6448588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, undefined
orthologous variants: 152215794-G-A

6448762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 152215547-A-G

http://identifiers.org/hco/1/GRCh38#6448765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215544-C-A

6448765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 152215544-C-T

http://identifiers.org/hco/1/GRCh38#6448849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215460-C-A

6448849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 152215460-C-T

http://identifiers.org/hco/1/GRCh38#6448852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215457-C-A

6448852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 152215457-C-T

http://identifiers.org/hco/1/GRCh38#6448920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215389-C-A

6448920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 152215389-C-G

6448920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 152215389-C-T

6448961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152215348-G-A

6448961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152215348-G-C

6448961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152215348-G-T

http://identifiers.org/hco/1/GRCh38#6448974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215341-C-A

6448974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 152215341-C-G

6448974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 152215341-C-T

6449043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152215272-A-G

6449058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152215257-T-C

6449137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152215179-A-G

6449201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152215116-A-G

6449210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152215109-T-G

http://identifiers.org/hco/1/GRCh38#6449224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152215098-C-A

6449224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152215098-C-G

6449224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152215098-C-T

6450086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152214329-T-C

http://identifiers.org/hco/1/GRCh38#6450277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152214243-C-A

6450277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152214243-C-T

http://identifiers.org/hco/1/GRCh38#6450286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152214234-C-A

http://identifiers.org/hco/1/GRCh38#6450292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152214228-C-A

6450292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152214228-C-T

6450346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152214182-G-A

6450346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152214182-G-C

6450346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152214182-G-T

6450702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152213856-G-A

6450702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152213856-G-C

6450877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152213721-C-T

6450981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152213620-G-A

http://identifiers.org/hco/1/GRCh38#6451360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#152213235-C-A

6451360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 152213235-C-T

6451434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152213168-G-A

6451434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152213168-G-C

6451434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152213168-G-T

6451512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152213093-G-T

6451573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152213034-G-A

6451579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152213028-G-A

6451873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152212747-C-T

6451876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152212744-T-A

6451903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152212717-G-C

6451903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152212717-G-T

6452079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: missense variant
orthologous variants: 152212541-G-A

6452079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: stop gained
orthologous variants: 152212541-G-T

6453514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152211760-T-G

6453529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152211740-C-T

6453968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152211505-T-A

6454003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152211471-G-T

6454458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152211002-T-C

6454851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152210609-G-A

6454851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152210609-G-T

6455071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152210389-A-G

http://identifiers.org/hco/1/GRCh38#6455100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152210360-C-A

6455100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152210360-C-T

http://identifiers.org/hco/1/GRCh38#6455145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152210315-C-A

6455169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152210291-G-A

6455169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152210291-G-T

6455196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, stop_gained
orthologous variants: 152210264-G-T

6455253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152210207-G-A

6455253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152210207-G-T

6455499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152209958-G-T

6455511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 152209946-G-T

6455531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 152209926-G-A

6455602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152209843-A-G

http://identifiers.org/hco/1/GRCh38#6455614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152209831-C-A

6455614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152209831-C-T

6455634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152209811-A-G

http://identifiers.org/hco/1/GRCh38#6455712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152209733-C-A

6455712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 152209733-C-T

http://identifiers.org/hco/1/GRCh38#6455877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152209568-C-A

6455877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152209568-C-T

6455925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152209379-C-G

6455953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152209348-T-C

6455965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152209342-A-G

6455965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron_variant, missense_variant
orthologous variants: 152209342-A-T

6456263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 152209076-A-G

6456263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 152209076-A-T

6456283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152209059-G-A

6456283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152209059-G-T

6456293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152209048-G-A

http://identifiers.org/hco/1/GRCh38#6456347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152209002-A-C

6456347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152209002-A-G

http://identifiers.org/hco/1/GRCh38#6456396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152208953-C-A

6456396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152208953-C-G

6456396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152208953-C-T

http://identifiers.org/hco/1/GRCh38#6456481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152208905-C-A

6456481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152208905-C-G

6456481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152208905-C-T

http://identifiers.org/hco/1/GRCh38#6456642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152208764-C-A

6456642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152208764-C-G

6456642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152208764-C-T

http://identifiers.org/hco/1/GRCh38#6456699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152208718-C-A

6456757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208662-G-A

6456794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208624-G-T

6456802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208616-T-C

6456802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208616-T-G

6456805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208614-G-A

http://identifiers.org/hco/1/GRCh38#6457063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152208401-C-A

6457072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208392-G-A

6457072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208392-G-T

6457082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208382-A-G

6457139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208298-T-C

6457325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208119-G-A

6457398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208046-G-A

6457422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208023-G-A

6457422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208023-G-C

6457422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152208023-G-T

http://identifiers.org/hco/1/GRCh38#6457447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152207995-C-A

6457447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152207995-C-G

6457447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152207995-C-T

6458960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152206867-G-T

6458993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152206834-C-T

6459014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152206814-A-G

6459014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152206814-A-T

6459139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152206653-G-T

6459142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152206650-G-A

6459304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152206454-G-C

6459330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152206431-C-T

http://identifiers.org/hco/1/GRCh38#6459474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152206294-A-C

6459570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152206161-A-G

6459579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152206152-C-T

6459847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152205846-C-T

http://identifiers.org/hco/1/GRCh38#6459853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152205840-C-A

6459853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: intron variant
orthologous variants: 152205840-C-T

6460155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152205562-G-A

http://identifiers.org/hco/1/GRCh38#6460272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152205435-C-A

6460473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152205228-G-T

http://identifiers.org/hco/1/GRCh38#6460499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152205206-C-A

6460499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 152205206-C-T

6460803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152204898-G-A

6460803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152204898-G-T

6460824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152204877-G-T

http://identifiers.org/hco/1/GRCh38#6460871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152204834-C-A

http://identifiers.org/hco/1/GRCh38#6460877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152204828-A-C

6460877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152204828-A-G

6461026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152204686-A-G

6461088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152204623-G-A

6461088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152204623-G-T

http://identifiers.org/hco/1/GRCh38#6461118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#152204590-A-C

6461118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 152204590-A-G

6461158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 152204557-T-G

6461293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 152204434-G-A

6461293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 152204434-G-C

6461293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 152204434-G-T