21006372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88331910-C-G

21006374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88331912-G-A

21006374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88331912-G-C

21006374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88331912-G-T

21006463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332009-G-A

21006463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332009-G-C

21006474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332020-T-C

21006624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332143-T-C

http://identifiers.org/hco/9/GRCh38#21006628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88332147-C-A

21006799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332296-T-A

21006863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332356-T-A

21006863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332356-T-C

21006863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332356-T-G

21006876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332369-T-C

21006935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332400-A-G

21006935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332400-A-T

21006957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332425-A-G

21006957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332425-A-T

http://identifiers.org/hco/9/GRCh38#21007018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88332488-C-A

21007018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3 prime UTR variant
orthologous variants: 88332488-C-T

21007038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: undefined
orthologous variants: 88332502-C-T

21007058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: synonymous variant
orthologous variants: 88332522-G-A

21007058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: synonymous variant
orthologous variants: 88332522-G-T

21007125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 88332589-A-G

21007133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88332597-A-G

http://identifiers.org/hco/9/GRCh38#21007205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88332659-C-A

21007205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88332659-C-G

21007205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88332659-C-T

21007243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88332703-G-A

21007245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88332705-G-A

21007245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88332705-G-T

21007251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88332711-G-C

21007251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88332711-G-T

21007289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88332742-G-C

21007356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88332814-G-C

21007471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88332925-G-A

21007545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88332989-T-C

http://identifiers.org/hco/9/GRCh38#21007549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88332993-C-A

21007549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88332993-C-G

21007844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88337781-A-G

21007893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88337820-T-C

http://identifiers.org/hco/9/GRCh38#21007936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88337863-A-C

21007936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88337863-A-G

21007936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88337863-A-T

21007944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88337871-G-A

21007944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88337871-G-T

21007960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88337883-G-A

21007960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88337883-G-T

21007961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88337884-G-A

21007961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88337884-G-T

21008009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88337924-A-G

21008090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: missense variant
orthologous variants: 88338005-T-G

21008178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88338092-T-A

21008178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88338092-T-C

21008268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88338176-T-C

21008268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88338176-T-G

21008480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88338405-T-C

21008591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88338509-A-G

21008995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88339094-C-T

http://identifiers.org/hco/9/GRCh38#21009275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88339391-C-A

21009281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88339397-T-A

21009281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88339397-T-G

21009384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88339492-G-A

21009494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88339600-G-A

21009494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88339600-G-C

21010277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88340319-A-T

21011234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88340677-G-A

21011415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 88340854-C-T

21011449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, missense_variant
orthologous variants: 88341092-A-G

21011452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, missense_variant
orthologous variants: 88341094-G-T

21011490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 88341132-T-C

21011705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88341344-G-A

21011705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88341344-G-C

21011705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88341344-G-T

http://identifiers.org/hco/9/GRCh38#21011716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88341355-C-A

http://identifiers.org/hco/9/GRCh38#21011791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88341437-A-C

21011791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88341437-A-T

21011837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88341480-T-A

21011837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88341480-T-C

21011837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88341480-T-G

21012258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88341902-G-T

21013222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88342208-G-A

21013249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88342239-T-C

21013274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88342264-T-C

21013305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88342294-G-A

21013369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88342347-T-G

21013474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88342452-T-G

21013807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88342743-A-G

21014078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88342982-A-G

21014691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88343542-T-A

21014705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88343554-T-C

21014705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88343554-T-G

21014828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88343668-C-G

21014828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88343668-C-T

21014864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88343704-G-A

21014997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88343834-T-C

http://identifiers.org/hco/9/GRCh38#21015008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88343845-A-C

21015042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88343870-T-C

21015520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344455-G-T

http://identifiers.org/hco/9/GRCh38#21015523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88344458-C-A

21015523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344458-C-G

21015555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344503-A-G

http://identifiers.org/hco/9/GRCh38#21015594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88344536-C-A

21015618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344559-G-T

http://identifiers.org/hco/9/GRCh38#21015670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88344614-A-C

http://identifiers.org/hco/9/GRCh38#21015690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88344634-C-A

21015690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344634-C-T

21015695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344639-G-A

21015695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344639-G-C

21015695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344639-G-T

21015705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344649-G-A

21015705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344649-G-T

21015795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344734-T-C

21015809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344748-G-A

21015809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344748-G-T

21015816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344755-G-A

21015827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88344766-T-C

21015974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88345049-T-G

21015994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88345069-A-G

21016115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88345187-G-T

http://identifiers.org/hco/9/GRCh38#21016138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88345210-A-C

21016306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88345372-G-C

21016390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88345627-C-T

21016410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88345693-T-C

21016644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88345910-C-T

21016717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88345973-G-A

21016717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88345973-G-T

21016729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88345985-T-C

21016831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88346079-A-T

21016951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88346217-T-C

21017127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88346426-T-A

21017409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88346689-C-T

http://identifiers.org/hco/9/GRCh38#21017828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88347080-C-A

21017829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88347081-G-A

21017829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88347081-G-T

21017862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88347196-C-T

21017926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347290-T-C

21017932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347296-T-C

21017984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347342-G-T

21017994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347352-A-G

http://identifiers.org/hco/9/GRCh38#21017998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88347357-C-A

http://identifiers.org/hco/9/GRCh38#21018003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88347362-C-A

http://identifiers.org/hco/9/GRCh38#21018053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88347406-C-A

21018053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347406-C-T

http://identifiers.org/hco/9/GRCh38#21018074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88347427-C-A

21018085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347438-G-A

21018085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347438-G-C

21018085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347438-G-T

21018144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347480-T-C

21018224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88347552-C-G

21018944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88348230-G-A

21019656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88349079-C-G

21019656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88349079-C-T

21019850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88349237-G-C

21020098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88349411-T-C

21020131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88349444-A-G

21020213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88349530-A-G

21020256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88349583-T-C

21020525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88349797-A-G

21020588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88349878-T-C

21024027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88350849-G-A

21024042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88350864-T-C

21024070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88350892-T-G

21024286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88351066-T-C

21024291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88351071-A-G

21024291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88351071-A-T

21024320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88351106-C-T

21024426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88351208-A-G

21024783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88351705-C-G

21024942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88351858-A-G

21025229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88352125-C-T

21025457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88352581-A-G

21026141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88352830-T-C

21026254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88352904-C-T

21026321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88352969-A-T

21026451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353088-G-A

21026451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353088-G-T

http://identifiers.org/hco/9/GRCh38#21026456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88353093-C-A

21026456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353093-C-T

21026533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353113-G-C

21026533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353113-G-T

21026552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353132-T-A

21026552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353132-T-C

21026552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353132-T-G

http://identifiers.org/hco/9/GRCh38#21026562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88353142-A-C

21026562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353142-A-G

http://identifiers.org/hco/9/GRCh38#21026563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88353143-C-A

21026563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353143-C-T

21026581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353161-G-A

21026581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88353161-G-T

21026653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88353233-T-C

21026701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88353281-A-G

21026747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88353330-C-T

21026757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88353340-A-G

http://identifiers.org/hco/9/GRCh38#21026766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88353349-C-A

21026787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88353370-T-C

21026844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88353416-A-G

21027000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88353601-C-T

21027336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88353907-A-G

21027387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88353959-G-A

21027431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88354003-C-T

21027495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88354066-G-A

21027546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88354117-T-G

21028466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88354862-T-C

21028509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88354905-C-T

21028543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88354930-G-A

21028589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88354976-T-C

21028838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88355252-G-A

21029128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88355530-C-G

21029128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88355530-C-T

21029164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88355558-T-A

21029164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88355558-T-C

21029164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88355558-T-G

21029205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88355620-G-A

21029205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88355620-G-T

http://identifiers.org/hco/9/GRCh38#21029234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88355638-C-A

http://identifiers.org/hco/9/GRCh38#21029266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88355669-A-C

21029266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88355669-A-G

21029272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88355675-A-G

21030510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88356131-G-C

21030522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88356144-T-C

21030668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88356267-T-C

21030668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88356267-T-G

21030671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88356269-G-C

21030678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88356276-C-G

21031025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88356628-T-C

21031211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88356768-C-T

21031312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88356859-C-T

21031318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88356865-G-T

21031355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: intron variant
orthologous variants: 88356914-G-C

21031491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88357019-G-A

21031491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 88357019-G-T

http://identifiers.org/hco/9/GRCh38#21031618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#88357132-C-A

21031618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20920
most severe consequence: 5 prime UTR variant
orthologous variants: 88357132-C-T