19816607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361469-T-A

19816607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361469-T-C

http://identifiers.org/hco/10/GRCh38#19816824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16361685-C-A

19816824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361685-C-T

19816835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361696-G-A

19816890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361751-G-A

http://identifiers.org/hco/10/GRCh38#19816891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16361752-C-A

19816891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361752-C-T

19816926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361774-T-G

19816929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361777-C-G

19816929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361777-C-T

19816937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361785-G-T

19816959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361807-A-G

19816959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361807-A-T

19817020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361869-G-A

19817020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: 5 prime UTR variant
orthologous variants: 16361869-G-T

http://identifiers.org/hco/10/GRCh38#19817092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16361949-C-A

19817092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: missense variant
orthologous variants: 16361949-C-G

19817097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: synonymous variant
orthologous variants: 16361954-G-A

19817097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: missense variant
orthologous variants: 16361954-G-T

http://identifiers.org/hco/10/GRCh38#19817099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16361956-C-A

19817099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: missense variant
orthologous variants: 16361956-C-G

19817099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: missense variant
orthologous variants: 16361956-C-T

19817157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: synonymous variant
orthologous variants: 16362014-G-A

http://identifiers.org/hco/10/GRCh38#19817254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16362107-C-A

19817254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16362107-C-G

19817254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16362107-C-T

19817315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16362170-G-A

19817315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16362170-G-T

19817600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16362457-G-T

19817699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16362555-A-G

19817790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16362635-T-C

19817927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16362791-G-A

19817928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16362793-G-A

http://identifiers.org/hco/10/GRCh38#19818004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16362869-C-A

19818109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16362977-T-C

19818296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16363124-G-A

19818359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16363192-G-A

19818386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16363212-T-A

19818414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16363239-A-G

19818459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16363284-T-C

19819159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16363908-G-T

19819518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, undefined
orthologous variants: 16364225-C-G

http://identifiers.org/hco/10/GRCh38#19819965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16364651-A-C

19820148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16364785-G-T

19820156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16364793-A-T

19821377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16365270-G-T

19824361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367104-T-C

19824389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367132-G-T

19824391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367134-A-G

19824435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367178-A-G

19824442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367185-A-G

19824557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367356-T-C

19824559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367358-C-T

19824623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367408-A-G

19824663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367448-G-C

19824688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367471-A-G

19824710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367493-G-C

19824716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367499-T-C

19824718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367501-C-T

19824719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367502-A-G

19824744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367529-G-A

19825069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16367787-T-C

19826025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16368071-A-G

19826031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16368077-T-A

19826916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, undefined
orthologous variants: 16368434-G-A

19827379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16368903-G-A

19827379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16368903-G-C

19827452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16368978-T-C

19827898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16369638-C-G

19827977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16369717-A-T

19828116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16369843-A-G

19828439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16370749-C-T

19828607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16370920-A-G

19828677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16370991-A-G

19828766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16371081-A-G

19828768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16371083-T-G

19828927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16371600-A-T

19829007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16371671-G-A

19829007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16371671-G-C

19829119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16371772-A-G

19829119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16371772-A-T

19829171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16371811-T-C

19829241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16371880-A-G

19829291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16371946-A-G

19829329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16371993-C-T

19829383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16372050-T-C

19829421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16372086-G-A

19829421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16372086-G-T

19830186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16372650-G-T

19830414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16372894-A-G

19830497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16372963-T-C

19830536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16373001-T-C

19830555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16373020-A-G

19830738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: -A-G

19830758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: -A-G

19830758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: -A-T

19830767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16373562-A-G

19830784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16373579-C-G

19830882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16373670-G-A

19830985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16373765-G-A

19830985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16373765-G-T

19831209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16373929-T-C

19831313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16373995-C-T

19831367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16374049-A-G

19831386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16374064-C-T

19831396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16374074-G-A

19831397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16374075-G-A

19832360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16374424-A-G

19832369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16374433-G-A

http://identifiers.org/hco/10/GRCh38#19832379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16374443-A-C

19832478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16374855-T-C

19832525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16374906-T-C

19832566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16374948-A-T

19832604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16374984-C-T

19832622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16375001-T-C

19833744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16376489-A-G

19833783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16376528-G-C

19833867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16376596-A-G

19833875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16376604-C-T

19834153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16376865-G-T

19834893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16377293-A-T

19834938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16377329-A-G

19835265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16377637-G-A

19835563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16377884-G-A

19835563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16377884-G-T

19835673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16377984-G-T

19835689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16378001-G-A

19835689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16378001-G-C

19835696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16378008-A-T

19836223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16378181-A-G

19836324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16378263-A-G

19836339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16378280-A-G

19836414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16378352-A-G

19836510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16378446-A-G

19836646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16378572-A-G

19836683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16378609-C-T

http://identifiers.org/hco/10/GRCh38#19836709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16378633-A-C

19836742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16378656-T-C

19837094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16378984-G-C

http://identifiers.org/hco/10/GRCh38#19837186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16379071-C-A

19837186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379071-C-G

19837186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379071-C-T

19837237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379117-T-C

19837241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379121-A-G

19837290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379169-T-A

19837290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379169-T-C

19837334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379209-G-A

19837413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379393-T-A

19837413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379393-T-C

19837424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379404-G-A

19837727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379780-G-T

19837755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379808-T-C

19837829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379882-G-A

19837851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379898-T-C

19837914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379981-G-A

19837929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16379996-C-T

19842735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16390809-G-T

19842762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16390836-T-C

19842766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16390840-C-T

19842767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16390841-G-A

19844966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16391547-G-T

http://identifiers.org/hco/10/GRCh38#19845094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16391693-A-C

19845094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16391693-A-G

19845177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16391773-C-G

19845413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16392002-T-C

19846250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16392256-G-A

19846250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16392256-G-T

19846253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16392259-G-A

19846311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16392285-C-G

19846311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16392285-C-T

19846313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16392287-C-T

19847006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16393086-A-T

http://identifiers.org/hco/10/GRCh38#19847192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16393212-A-C

19847202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16393222-G-A

19847244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16393264-G-A

19847250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16393270-G-A

19847344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16393342-T-C

19847645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16393602-C-T

19847755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16393708-G-A

19847755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16393708-G-T

http://identifiers.org/hco/10/GRCh38#19848297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16393843-C-A

19848334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16393888-G-A

19848334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16393888-G-T

http://identifiers.org/hco/10/GRCh38#19848444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16393990-C-A

19848630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16394137-T-C

19848676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16394179-T-C

19848861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16394375-A-G

19848861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16394375-A-T

19848923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16394460-A-G

19849020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16394723-A-G

19849178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16394883-T-C

19849254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16394972-T-C

19849292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16395003-A-G

19849298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16395009-G-A

19849577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16395276-C-G

19849635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16395322-C-G

19849741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16395446-A-G

19849766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16395471-C-T

19849802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16395498-T-C

http://identifiers.org/hco/10/GRCh38#19849971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16395715-C-A

19850089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16395828-C-T

19850143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16395878-G-C

19850231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16395963-T-C

19850232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16395964-A-G

19850294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396032-A-T

19850381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396113-A-G

19850492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396226-A-G

http://identifiers.org/hco/10/GRCh38#19850563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16396291-C-A

19850563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396291-C-G

19850564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396292-T-C

19850604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396325-C-T

19850672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396388-G-A

19850694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396408-A-G

http://identifiers.org/hco/10/GRCh38#19850793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16396507-A-C

19850793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396507-A-G

19850793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396507-A-T

19850852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396567-T-G

19850962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396658-A-G

http://identifiers.org/hco/10/GRCh38#19850983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16396679-A-C

19851097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396829-G-A

19851097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16396829-G-T

19853092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16399996-A-T

19853178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16400069-A-G

http://identifiers.org/hco/10/GRCh38#19853204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16400095-C-A

19853279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16400172-T-G

19854246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16401931-G-A

19854246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16401931-G-T

19854540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16402207-A-G

19854615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16402329-G-A

19854615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16402329-G-C

http://identifiers.org/hco/10/GRCh38#19854657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16402364-C-A

19854689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16402404-C-G

19854775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16402489-T-C

19855356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16402903-C-T

19856699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16404200-G-A

19856969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16404442-T-A

19856973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16404446-G-A

19856973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16404446-G-C

19857055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16404529-C-T

19857171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16404652-C-T

http://identifiers.org/hco/10/GRCh38#19857194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16404675-C-A

19857194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16404675-C-T

19857235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16404711-C-G

19857241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16404717-A-G

19857267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16404743-G-A

19857674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16405136-G-A

19857683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16405148-T-C

19861360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16405255-A-G

http://identifiers.org/hco/10/GRCh38#19861381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16405279-A-C

19861582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16405471-T-C

19861681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16405568-C-T

19861696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16405583-A-G

http://identifiers.org/hco/10/GRCh38#19861707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16405595-C-A

19861754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16405641-C-T

19861900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16405780-T-C

19861902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16405782-G-A

19862343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16406272-T-C

19862954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16408652-A-G

19863060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16409996-G-T

19863134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16410104-A-G

http://identifiers.org/hco/10/GRCh38#19863208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16410175-C-A

19863311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16410281-A-G

19863352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16410322-T-C

19863381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16410351-G-A

19863381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16410351-G-T

http://identifiers.org/hco/10/GRCh38#19863428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16410399-C-A

19863429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16410400-T-C

19863465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16410436-A-G

19863551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16410519-T-C

19863679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16410674-A-G

19863804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16410808-T-A

http://identifiers.org/hco/10/GRCh38#19863837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16410844-A-C

19863840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16410847-G-A

http://identifiers.org/hco/10/GRCh38#19864005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16411002-A-C

19865170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16411756-T-C

http://identifiers.org/hco/10/GRCh38#19865220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16411798-C-A

19865599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16412218-G-A

19865645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16414258-T-C

19865702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16414314-A-G

19866033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16414640-T-A

19868068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16416264-G-T

19868496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16416407-C-T

19868548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16416452-G-T

19868595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16416817-A-G

19868715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16416934-A-G

19868715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16416934-A-T

19868755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16416976-T-C

19868760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16416981-A-G

19868760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16416981-A-T

19869567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16417369-A-G

19869615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16417414-G-A

19869620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16417419-G-C

19869671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16417471-A-T

19870070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16417802-A-T

19870093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16417824-T-C

19870097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16417828-G-A

19870102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16417833-G-A

19870106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16417837-A-T

19870137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16417869-T-A

19871931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16418636-C-T

19871962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16418667-G-A

19872160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16418830-C-G

19872259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16418928-A-G

19872306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16418971-G-A

19872578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16419222-G-A

19872579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16419223-G-A

19872860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16419513-C-T

19872861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16419514-G-A

19872905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16419558-G-A

19873890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16420867-C-G

19873942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16420915-T-C

19874233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16421362-G-C

19874319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16421461-C-G

19874362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16421549-T-G

19874487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16421662-A-G

19874691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16421834-G-C

19874708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16421860-A-G

19874747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16421898-T-C

19874750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16421902-G-C

19874824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16422018-C-T

http://identifiers.org/hco/10/GRCh38#19874826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16422020-C-A

19874826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16422020-C-G

19874826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16422020-C-T

19874832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16422026-A-T

19874860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16422054-G-A

http://identifiers.org/hco/10/GRCh38#19874963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16422155-A-C

19875001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16422182-G-A

19875025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16422206-C-T

19875122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16422302-G-A

19875528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16422707-G-A

19875747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16423327-G-A

19875803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16423374-G-A

19875852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16423423-C-G

19875905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16423476-T-C

19876041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16423603-G-A

19876199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16423727-G-T

19876314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16423825-C-G

19876367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16423891-C-T

19876830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16424281-G-C

http://identifiers.org/hco/10/GRCh38#19876933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16424387-C-A

19876933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16424387-C-T

19876934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16424388-G-A

19877083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16424523-G-A

19877150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16424586-A-G

19883647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16425842-A-G

19883658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16425853-G-A

http://identifiers.org/hco/10/GRCh38#19887641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16426725-A-C

19887641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16426725-A-G

19887646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16426730-C-T

19887691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16426771-G-T

19888048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16427081-C-T

19888072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16427098-C-T

19888083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16427109-T-C

19888276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16427433-G-A

19889042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16428523-T-A

19889153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16428627-A-G

19889680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16429132-A-G

19889725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16429176-C-T

19889796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16429232-G-C

19889815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16429251-A-T

19889826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16429262-G-C

19889826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16429262-G-T

19890048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16430142-G-T

19891118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16430655-C-T

19891154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16430692-G-A

19891180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16430718-G-T

19891262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16430791-T-C

19891374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16430899-C-T

19891462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16430984-A-G

19891522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16431046-T-C

19891586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16431109-C-G

19891586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16431109-C-T

19891592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16431115-C-T

19891849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16431366-A-G

19891946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16431464-A-G

19892030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16431552-G-A

http://identifiers.org/hco/10/GRCh38#19892148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16431673-A-C

19892332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16431828-C-T

19892371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16431868-G-T

19892461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16431936-A-G

19892524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16431999-C-T

19893935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16433525-T-A

http://identifiers.org/hco/10/GRCh38#19896094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16436441-C-A

19896112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16436472-C-G

19900389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16443447-C-T

http://identifiers.org/hco/10/GRCh38#19900489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16443529-C-A

19906955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16444499-G-A

19907121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16444658-G-A

http://identifiers.org/hco/10/GRCh38#19907193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16444726-C-A

19907207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16444739-A-G

19907373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445053-G-A

19907373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445053-G-C

19907374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445054-T-C

19907376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445056-C-T

http://identifiers.org/hco/10/GRCh38#19907411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16445124-A-C

19907411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445124-A-G

19907441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445157-G-A

19907473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445187-G-T

19907529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445248-A-T

http://identifiers.org/hco/10/GRCh38#19907591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16445310-C-A

19907591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445310-C-G

19907596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445315-T-C

http://identifiers.org/hco/10/GRCh38#19907626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16445351-A-C

19907626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445351-A-G

19907996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445529-G-A

19907996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445529-G-T

19908010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445543-G-C

19908135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445661-G-C

19908361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445880-T-C

19908396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16445915-G-C

http://identifiers.org/hco/10/GRCh38#19908531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16446044-A-C

19908542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16446054-C-T

19908602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16446114-C-G

19908623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16446136-G-A

19908640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16446152-A-T

19908838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16447057-G-A

19908942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16447159-A-G

http://identifiers.org/hco/10/GRCh38#19909040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16447258-A-C

19909040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16447258-A-G

19909246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16447409-C-T

19909253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16447432-C-T

19909619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16447785-T-C

19909773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16447862-T-C

19909917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16447998-T-C

19910168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16448219-T-A

19910174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16448225-A-G

19910204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16448237-G-T

19910292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16448308-T-C

19910305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16448321-C-T

19911041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16448985-A-G

19911062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16449005-C-T

19911124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16449049-G-A

19911226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16449143-A-G

19911226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16449143-A-T

19911237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16449155-C-T

19911512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16449742-G-A

19911512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16449742-G-T

19911587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16449816-C-G

19911611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16449838-C-T

19911742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16449970-C-T

19911743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16449971-A-G

19911754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16449982-C-T

19911774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16450002-T-C

19911843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16450064-T-C

19911959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16450165-A-G

19911968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16450174-T-C

19911978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16450184-T-G

19912118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16450423-G-A

19912132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16450437-T-C

19912181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16450487-A-G

19912237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16450534-T-C

19912280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16450590-T-C

19912315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16450626-A-T

19912337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16450648-G-A

19917717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16452291-A-G

19917718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16452292-T-C

19917927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16452512-C-T

19917953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16452536-G-A

19917969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16452548-G-C

http://identifiers.org/hco/10/GRCh38#19918011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16452594-C-A

http://identifiers.org/hco/10/GRCh38#19918163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16452830-A-C

19918235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16452902-G-A

19918375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16453013-C-G

19918375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16453013-C-T

19918496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16453127-C-G

19918496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16453127-C-T

19918516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16453152-T-C

19918521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16453157-T-A

19918618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16453253-G-A

19919193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16453783-C-G

19919201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16453792-C-T

19919207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16453798-A-G

19919212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16453803-G-A

19919609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16454239-A-G

19919609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16454239-A-T

19919614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16454244-T-G

19919764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16454521-G-T

19919883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16454619-T-C

19919885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16454621-G-T

19919917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16454653-T-C

19919917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16454653-T-G

19919951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16454691-T-C

19921289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16455187-T-C

19921362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16455252-T-G

19921401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16455287-G-A

19921763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16455610-G-A

19922548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16456036-G-C

19922771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16456276-G-A

19922967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16456461-A-G

19922974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, undefined
orthologous variants: 16456468-T-C

19923376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16457226-C-T

19923413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16457263-G-A

19923503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16457353-A-G

19924836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16458404-A-G

19924951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16458525-A-G

19924951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16458525-A-T

19924992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16458559-G-T

19925154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16458719-G-A

19925201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16458765-G-A

19925567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16459142-G-A

19925567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16459142-G-C

19925573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16459146-T-A

19928521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16459456-G-T

19928570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16459698-G-A

19928583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16459711-G-A

19928583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16459711-G-T

19928608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16459733-G-T

19929257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16459994-C-T

19929398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16460124-G-A

19930151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16461036-G-A

19930201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16461086-T-A

19930286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16461162-A-G

19930333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16461209-G-A

http://identifiers.org/hco/10/GRCh38#19930582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16461450-A-C

19930582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16461450-A-G

http://identifiers.org/hco/10/GRCh38#19931470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16461884-A-C

19931470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16461884-A-G

19931750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16462144-G-A

19931858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16462247-T-C

19932199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16462719-T-C

19932426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16462953-G-A

19932938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16463468-C-G

19932949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16463479-G-C

http://identifiers.org/hco/10/GRCh38#19932984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16463514-A-C

19935135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16464327-A-G

19935189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16464381-G-A

19935234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16464425-G-A

19935237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16464428-C-T

19935251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16464442-G-A

19935261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16464452-G-A

19935387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16464575-G-A

http://identifiers.org/hco/10/GRCh38#19935408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16464596-C-A

19935487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16464664-G-A

19935660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16464807-T-A

19935660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16464807-T-C

19937367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16465524-G-A

19937419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16465565-C-T

http://identifiers.org/hco/10/GRCh38#19937595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16465680-A-C

19937629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16465705-T-C

19937647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16465727-C-G

19937744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16465822-G-A

19938249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16466284-C-T

19938788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16466424-A-T

19938810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16466446-G-T

19938892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16466525-C-T

19939039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16466664-A-T

19939324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16466936-G-A

19939481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16467092-C-T

19939555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16467150-A-G

19939573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16467167-T-C

19939664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16467251-T-C

19939739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16467265-G-A

19940063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16467536-T-C

19940121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16467593-G-T

http://identifiers.org/hco/10/GRCh38#19940188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16467660-A-C

19940208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16467680-A-G

http://identifiers.org/hco/10/GRCh38#19940330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16467795-C-A

19940330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16467795-C-T

19940463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16467890-C-T

19940477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16467904-T-C

19940526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16467951-T-A

19941849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16470302-G-A

19941933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16470377-C-T

19941998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16470458-G-A

19941998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16470458-G-T

19942008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16470468-T-G

19942112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16470568-A-G

19942242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16470672-C-T

19942303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16470732-G-T

19942340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16470773-G-T

19942406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16470833-C-T

19942478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16470906-T-C

19945294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16471337-T-C

19945528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16471571-G-T

19946209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16472231-C-G

19946209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16472231-C-T

19946230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16472252-G-A

19946237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16472259-T-C

19946273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16472295-G-A

19947332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16472751-T-C

19947492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16472921-T-A

19947525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16472954-G-A

19947579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16472983-A-G

http://identifiers.org/hco/10/GRCh38#19947732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16473133-C-A

19947732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473133-C-G

19947732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473133-C-T

19947755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473154-T-C

19947760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473159-A-T

19947788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473196-G-T

19948049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473429-G-T

19948103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473477-T-C

19948134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473507-A-G

19948171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473543-C-T

19948316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473685-G-A

19948470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473834-A-T

19948507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473872-A-G

19948559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473927-A-G

19948727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16473993-G-T

19948752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16474010-T-G

19949569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16474576-G-A

19949625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16474616-A-G

19949681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16474668-A-G

19949681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16474668-A-T

19952450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16476559-C-T

19952650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16476747-A-G

19953291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16477299-G-T

19953309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16477317-G-A

19953388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16477393-G-T

19953622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16477644-G-T

19954039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16478060-G-C

http://identifiers.org/hco/10/GRCh38#19954236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16478207-A-C

http://identifiers.org/hco/10/GRCh38#19954264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16478235-A-C

19954264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16478235-A-G

19956940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16482250-A-G

http://identifiers.org/hco/10/GRCh38#19956953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16482263-C-A

19956996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16482304-G-A

19957102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16482407-G-T

19957106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16482411-T-G

19960525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16483097-C-T

19960816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16483376-T-C

19960851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16483407-G-A

19960851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16483407-G-T

19960954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16483522-G-A

19960954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16483522-G-C

19960996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16483583-G-T

19961067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16483642-G-A

19961158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16483735-G-T

19961162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16483739-T-C

19961250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16483817-G-A

19961330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16483865-A-G

19961531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16484076-C-T

19961574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16484127-C-G

19961594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16484145-G-A

19961723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16484288-T-C

19961849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16484395-C-T

19962054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16484607-A-G

19963036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16485535-G-T

19963059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16485554-C-T

19963060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16485555-C-T

19963105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16485599-C-T

19963293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16485775-G-A

19963328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16485807-C-T

19965683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486046-G-A

19965685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486048-G-A

19965900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486251-C-T

19965924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486275-C-T

19965926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486277-C-T

19966054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486406-C-T

http://identifiers.org/hco/10/GRCh38#19966417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16486474-A-C

19966417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486474-A-T

http://identifiers.org/hco/10/GRCh38#19966421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16486478-A-C

19966421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486478-A-T

19966432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486489-G-A

19966432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486489-G-T

http://identifiers.org/hco/10/GRCh38#19966435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16486492-C-A

19966435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486492-C-G

19966439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486496-T-A

19966439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486496-T-C

19966439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486496-T-G

19966458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486506-T-A

19966458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486506-T-C

19966458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486506-T-G

19966460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486508-T-A

19966460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486508-T-G

19966462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486510-T-A

19966462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486510-T-C

19966462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486510-T-G

http://identifiers.org/hco/10/GRCh38#19966464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16486512-C-A

19966464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486512-C-G

19966464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486512-C-T

19966558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486567-C-G

19966558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16486567-C-T

19966876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, undefined
orthologous variants: 16488864-A-G

19966876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, undefined
orthologous variants: 16488864-A-T

19967028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, undefined
orthologous variants: 16489003-G-A

19967105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16489080-C-G

http://identifiers.org/hco/10/GRCh38#19967129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16489091-A-C

19967420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16489356-T-C

19967527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16489468-A-T

19967552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16489496-A-G

19967637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16489571-T-C

19967830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16490210-G-A

19967970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16490336-A-G

19968105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16490480-G-A

19968312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16490644-T-A

19968312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16490644-T-C

19968312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16490644-T-G

19968642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16490730-C-T

19968658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16490731-A-T

http://identifiers.org/hco/10/GRCh38#19969055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16491075-C-A

19969583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16491570-G-T

19969683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16491671-C-T

19969700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16491689-T-C

19969842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16491817-A-T

19970017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16491992-A-T

19970032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16492007-T-C

19970220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16492212-A-G

19970293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16492281-G-T

19970429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16492417-A-G

19971525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16494267-G-A

19971998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16494686-T-C

19972715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16494904-G-A

19973023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16495182-T-A

http://identifiers.org/hco/10/GRCh38#19973205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16495330-C-A

19973690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16495671-A-T

19973931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16495892-A-G

http://identifiers.org/hco/10/GRCh38#19973944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16495905-A-C

19974180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16496112-A-G

19974239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16496157-G-C

19974240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16496158-G-T

19974542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16496461-A-G

19974593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16496510-C-T

19978783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16496648-T-C

19978878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16496742-A-G

19978919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16496768-A-G

19978972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16496812-T-A

19979031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16496869-G-A

19979098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16496930-T-G

19979179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16497023-A-T

19979229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16497061-T-A

19979243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16497075-G-A

http://identifiers.org/hco/10/GRCh38#19979324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16497159-A-C

19979336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16497171-C-T

19979786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16497654-C-T

http://identifiers.org/hco/10/GRCh38#19980228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16498104-A-C

19980228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16498104-A-G

19980296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16498188-C-T

19980383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16498275-G-T

19980451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16498343-A-G

http://identifiers.org/hco/10/GRCh38#19980869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16498624-C-A

19980887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16498641-C-T

19981084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16498831-G-C

19981087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16498834-G-A

19981087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16498834-G-C

19981317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16498977-T-C

19981469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16499124-A-G

19981535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16499194-T-G

19981732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16499402-T-G

19982554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16499563-T-A

19982697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16499690-T-A

19982864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16499851-A-G

19983175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16500198-A-G

19983221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16500244-A-G

19983329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16500335-A-G

19984288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16501213-A-T

19984848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16501744-A-T

19985072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16501959-G-C

19985195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16502080-C-T

19985335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16502231-A-G

19985689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16502392-G-A

19986165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16502862-G-A

19986217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16502905-A-T

http://identifiers.org/hco/10/GRCh38#19986570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16503227-C-A

19986570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16503227-C-G

19986592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16503243-G-A

19986592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16503243-G-C

19986592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16503243-G-T

19986683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16503334-T-C

19986710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16503346-T-A

19986736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16503372-C-G

19986736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16503372-C-T

19988057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16504920-G-A

19988081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16504945-T-C

19988484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16505300-G-A

19988484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16505300-G-T

19990654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16505480-A-G

19990681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16505507-T-G

19990840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16505676-T-G

19990875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16505711-C-T

http://identifiers.org/hco/10/GRCh38#19990888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16505724-A-C

19990896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16505732-T-G

19992044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16508097-T-A

19992044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16508097-T-C

19992229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16508329-T-C

19992272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16508372-A-G

19992312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16508420-T-G

19992532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16508645-A-G

19992619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16508725-C-T

19992833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16508883-C-T

19992886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16508932-T-C

19993071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16509117-A-G

19995650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16510796-G-C

19995692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16510835-G-T

19995698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16510841-T-G

19995843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16510941-G-T

19997074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16511166-C-G

19997074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16511166-C-T

19997210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16511307-G-A

19997227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16511326-G-A

19997227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16511326-G-C

19997369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16511468-C-T

19997387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16511489-T-C

19997890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16512884-G-A

19997945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16512947-T-C

19998120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16513116-T-C

19998262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16513259-T-G

19998263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16513260-G-A

19998313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16513310-T-G

19998315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16513312-A-T

19998479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16513473-G-A

19998479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16513473-G-T

19998734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16513758-A-G

19998844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16513922-C-T

19999053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16514115-G-A

19999075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16514137-G-A

19999117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16514168-G-T

19999160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16514194-A-G

19999289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16514318-G-A

19999299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16514328-G-A

19999881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16514842-A-T

19999922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16514883-G-A

19999943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16514902-C-T

19999946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16514905-A-G

20000118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16515034-G-T

20000181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16515095-G-A

20000323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16515216-A-G

20000451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16515319-G-A

20000535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16515364-T-C

20000535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16515364-T-G

20000684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16515476-G-A

20000728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16515516-C-T

20000730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16515518-G-T

20000819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16515608-G-A

20000925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16515714-G-A

20000940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16515729-C-T

20001518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16516306-G-A

20001521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16516309-G-A

20001602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16516400-A-G

20001781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: missense variant
orthologous variants: 16516839-A-G

20001893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: synonymous variant
orthologous variants: 16516951-G-A

20001893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: synonymous variant
orthologous variants: 16516951-G-T

20001931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: missense variant
orthologous variants: 16516989-G-A

20001931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: missense variant
orthologous variants: 16516989-G-C

http://identifiers.org/hco/10/GRCh38#20001935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16516993-C-A

http://identifiers.org/hco/10/GRCh38#20001944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16517002-C-A

20001944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: missense variant
orthologous variants: 16517002-C-G

20001944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: synonymous variant
orthologous variants: 16517002-C-T

20002123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16517166-G-A

20002123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16517166-G-C

20002123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16517166-G-T

http://identifiers.org/hco/10/GRCh38#20004898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16518438-A-C

20004943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16518477-G-C

20005013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16518548-C-G

20005086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16518633-A-G

20006501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16519293-C-T

20007076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16519788-C-T

20007104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16519815-T-C

20007300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16520017-C-T

20010582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16523510-T-C

20010604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16523489-T-C

20010938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16522166-C-T

20012708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16525178-T-A

http://identifiers.org/hco/10/GRCh38#20012796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16525247-A-C

20012796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16525247-A-T

20012815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16525266-C-T

20012820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16525271-A-G

20012834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16525285-G-A

20012858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16525314-T-C

20012895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16525380-G-A

20012914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16525399-G-A

20012955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16525438-T-C

20013082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16526545-A-G

20013104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16526567-G-C

20013132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16526595-T-C

20013442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16526893-T-G

20013474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16526929-A-T

20013498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16526952-G-A

20013498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16526952-G-T

20013523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16526976-T-C

20013581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16527023-A-G

http://identifiers.org/hco/10/GRCh38#20013589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16527031-C-A

20013607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16527046-T-C

20013656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16527093-A-G

20013690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16527126-G-C

20013820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16527232-G-A

20013828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16527240-A-G

20013940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16527337-G-A

20013944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16527341-C-T

http://identifiers.org/hco/10/GRCh38#20014044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16527598-C-A

http://identifiers.org/hco/10/GRCh38#20017046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16528326-A-C

20017046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16528326-A-T

20017117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16528398-A-G

http://identifiers.org/hco/10/GRCh38#20017186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16528464-C-A

20017233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16528511-C-T

20017236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16528514-G-A

20017237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16528515-C-T

20017312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16528581-T-C

20017327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16528596-G-A

20017400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16528663-C-T

20017476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16528740-C-G

20017477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16528741-C-T

20017571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16529854-G-A

20018942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16530679-G-T

20019402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16531038-T-C

20019431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16531065-G-T

20019521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16531149-T-C

20019521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16531149-T-G

20019656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16531304-C-G

20019656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16531304-C-T

20019808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16531444-G-A

http://identifiers.org/hco/10/GRCh38#20019899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16531512-A-C

20019899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16531512-A-G

20019961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16531573-A-G

20020129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16531648-A-G

20020283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16531691-G-T

20020692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16532023-C-G

20020917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16532248-G-C

20021004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16532324-G-A

20021140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16532439-G-T

20022424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16533153-G-A

http://identifiers.org/hco/10/GRCh38#20022544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16533260-C-A

20022544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16533260-C-T

20022633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16533357-C-G

20022718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16533436-G-A

20023071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16533892-C-T

20023304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16534009-C-T

20023305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16534010-A-G

20024068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16536225-A-G

http://identifiers.org/hco/10/GRCh38#20024215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16536376-A-C

20024215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16536376-A-G

20024288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16536449-A-G

20024312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16536470-C-T

20024334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16536491-G-T

http://identifiers.org/hco/10/GRCh38#20024335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16536492-C-A

20025777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16536686-A-G

20025860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16536760-A-G

20026252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16537778-A-G

20026271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16537797-T-C

20026311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16537842-C-T

20026351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16537867-A-G

20026451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16537964-T-C

20027653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16538597-T-C

20027660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16538604-T-C

20027671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16538615-G-T

http://identifiers.org/hco/10/GRCh38#20027869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16538767-A-C

20028207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16539108-A-T

20028242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16539187-C-T

20028270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16539217-G-A

20028410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16539361-G-A

20028410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16539361-G-C

20028432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16539386-A-G

20028446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16539400-A-G

http://identifiers.org/hco/10/GRCh38#20028447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16539401-C-A

20028466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16539408-G-C

20028466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16539408-G-T

20028495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16539440-T-C

20028498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16539443-A-G

20028557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16539498-G-A

20029304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16540266-A-G

20029307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16540269-A-G

http://identifiers.org/hco/10/GRCh38#20029859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16540786-C-A

20035246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16543106-A-G

20035265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16543124-C-G

20035293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16543152-G-A

20035311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16543170-T-A

20035311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16543170-T-C

20035314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16543173-A-G

20035970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16543533-A-G

20036180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16543732-A-T

20036321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16543877-C-G

20036321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16543877-C-T

20036396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16543947-T-G

20036417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16543971-G-A

20039330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16546577-G-A

20039370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16546618-C-T

20039472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16546712-G-A

http://identifiers.org/hco/10/GRCh38#20039518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16546756-C-A

20040963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16547440-T-C

http://identifiers.org/hco/10/GRCh38#20042056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16549124-C-A

20042281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16549317-G-T

20042538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16549552-G-A

20042555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16549569-T-G

20042575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16549589-A-G

20042787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16549756-T-C

http://identifiers.org/hco/10/GRCh38#20042852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16549822-C-A

20042852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16549822-C-G

20043084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16550054-C-T

20043088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16550058-T-A

20043238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16550208-T-C

20043246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron variant
orthologous variants: 16550216-G-A

20043432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16550489-T-G

http://identifiers.org/hco/10/GRCh38#20043483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16550540-C-A

20043494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16550550-A-G

20043561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16550582-G-A

20043561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16550582-G-T

http://identifiers.org/hco/10/GRCh38#20043579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16550600-A-C

20044666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16550891-G-T

http://identifiers.org/hco/10/GRCh38#20044939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16551128-A-C

20044950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16551139-G-A

20045069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16551239-T-G

http://identifiers.org/hco/10/GRCh38#20045550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16551442-A-C

20045710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16551598-C-G

20045732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16551620-C-G

20045808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16551699-T-A

20046084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16552527-A-G

20046107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16552549-A-G

20046209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16552662-A-T

20046212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16552665-G-C

http://identifiers.org/hco/10/GRCh38#20046732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16552793-C-A

20046732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16552793-C-T

http://identifiers.org/hco/10/GRCh38#20046849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16552908-A-C

20046849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16552908-A-G

20046849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16552908-A-T

20047058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16553117-A-G

http://identifiers.org/hco/10/GRCh38#20047143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16553143-C-A

20047143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16553143-C-T

20047506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16553459-A-G

20047526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16553479-A-G

20047683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16553629-G-A

20052545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16554287-C-T

http://identifiers.org/hco/10/GRCh38#20052562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16554301-C-A

20052662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16554409-C-T

20052695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16554442-G-A

20052695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16554442-G-T

20052709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16554456-T-A

20052709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16554456-T-G

20052844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16554561-A-G

20052884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16554603-C-T

20053069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16554779-C-T

20053070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16554780-C-T

20053238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16554942-C-T

20053277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16554979-T-G

http://identifiers.org/hco/10/GRCh38#20053331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16555041-C-A

20053509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16555215-A-T

20053602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16555309-C-T

http://identifiers.org/hco/10/GRCh38#20053854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16555555-C-A

20053854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16555555-C-T

20053977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16555675-A-G

http://identifiers.org/hco/10/GRCh38#20054893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16556589-A-C

20055050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16556731-A-G

20058351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16558787-C-T

20058364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16558800-A-T

20058474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16558897-T-C

20058487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16558910-T-G

20058504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16558927-A-G

20058544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16558967-A-G

20058555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16558978-C-T

20058569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16558992-A-G

20058574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16558997-G-A

20058660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559059-G-A

20058673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559072-C-T

http://identifiers.org/hco/10/GRCh38#20058698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16559090-C-A

20058698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559090-C-G

20058698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559090-C-T

20058765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559169-C-G

20058858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559240-G-A

20058936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559323-G-A

20058949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559336-A-G

20058991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559379-T-C

20059045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559433-G-C

20059050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559438-G-C

20059119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559513-G-A

20059242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559713-C-G

20059242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559713-C-T

20059274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16559777-G-A

http://identifiers.org/hco/10/GRCh38#20059526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16560144-A-C

20059549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16560165-T-A

20059567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16560184-G-C

20059569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16560186-G-A

20059596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16560213-A-T

20059607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16560224-G-A

20059646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16560264-A-G

20059673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16560291-C-T

20059754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16560373-G-C

20059784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16560405-A-G

20059876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16560494-C-T

20059910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16560523-T-A

20059910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16560523-T-G

http://identifiers.org/hco/10/GRCh38#20059935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16560550-C-A

http://identifiers.org/hco/10/GRCh38#20061980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16561798-A-C

20062006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16561829-C-G

20062029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16561850-C-G

20062061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16561883-A-G

20062085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16561907-G-A

20062101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16561923-T-C

20062106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16561928-A-T

20062553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16562377-A-G

20062555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16562379-G-C

20062684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16562483-G-A

http://identifiers.org/hco/10/GRCh38#20062713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16562510-A-C

20062776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16562581-C-G

20062776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16562581-C-T

20062885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16562677-A-G

20062913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16562687-A-G

20062973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16562724-A-G

20063085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16562823-G-A

20063085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16562823-G-T

20063281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16562853-C-T

20063291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16562863-G-T

20063764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16563605-G-A

20063904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16563740-T-C

20063907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16563743-T-C

20063907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16563743-T-G

20063984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16563802-T-A

20064009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16563817-G-C

20064009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16563817-G-T

20064066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16563911-T-C

20064100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16563961-C-G

20064215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16564059-A-G

20064215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16564059-A-T

20066332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16568342-A-G

20066347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16568356-A-G

20066855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16568843-T-C

20067228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16569447-G-C

20067228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16569447-G-T

20067342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16569556-G-A

http://identifiers.org/hco/10/GRCh38#20068027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16570001-C-A

20068027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16570001-C-T

20068104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16570080-G-A

20068104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16570080-G-C

20068104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16570080-G-T

20068148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16570125-T-C

20068254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16570231-A-G

20068254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16570231-A-T

http://identifiers.org/hco/10/GRCh38#20068257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16570234-C-A

20068287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16570264-G-A

20068324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16570300-G-A

20068324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16570300-G-T

20068599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16570593-G-A

20068865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16570792-T-C

20068986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16570911-G-C

20069258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16571197-C-T

20069302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16571241-G-A

20070205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16571597-G-C

20070532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16571958-A-G

20070568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16571997-G-T

http://identifiers.org/hco/10/GRCh38#20071775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16572351-A-C

20071827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16572400-G-A

20071852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16572424-T-G

20072823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16573131-T-C

20072942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16573229-A-G

20073055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16573340-A-G

http://identifiers.org/hco/10/GRCh38#20073240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16573518-A-C

20073287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16573565-C-T

20073504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16573811-C-T

20073514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16573821-T-C

20074052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574316-A-G

20074052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574316-A-T

http://identifiers.org/hco/10/GRCh38#20074057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16574321-A-C

20074067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574325-C-T

20074277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574511-T-C

20074302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574541-T-C

20074304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574543-A-G

20074304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574543-A-T

20074309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574548-G-C

20074552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574769-A-G

20074594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574811-A-G

20074594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574811-A-T

20074613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574829-C-G

20074713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574929-G-T

http://identifiers.org/hco/10/GRCh38#20074715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16574931-C-A

20074715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16574931-C-T

20075039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16575236-G-A

20075078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16575275-T-C

20075091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16575288-A-G

20075099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16575296-G-T

20075852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16575713-C-T

20075988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16575835-G-T

20076155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16575990-G-A

20076166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16576001-G-A

20076234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16577009-T-A

20076242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16577017-A-T

20076281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16577056-A-T

20076364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16577128-A-G

20076445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16577208-A-G

20076460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16577224-T-G

20076472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16577236-C-G

20076558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16577314-C-T

20076577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16577321-T-G

20076612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16577362-T-C

20076716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16577395-T-C

20076896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16577574-C-T

20077295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16578882-T-C

20083853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16581850-T-G

20084090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582082-A-T

20084273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582230-A-G

20084495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582384-G-C

20084511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582400-G-A

20084617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582489-A-G

20084678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582525-C-T

20084749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582596-G-A

20084782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582627-A-G

20084793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582637-T-G

20084804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582648-A-G

20085020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582819-G-A

20085054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582853-T-C

20085055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582854-G-A

20085086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582880-G-A

20085096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582890-C-G

20085123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582917-C-G

20085123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16582917-C-T

http://identifiers.org/hco/10/GRCh38#20085149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16582934-A-C

20085295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16583060-G-A

20085412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16583173-G-A

20085596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16583352-A-G

20085610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16583366-T-C

20085773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16583514-G-A

20085823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16583564-A-G

20085899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16583760-C-T

20085907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16583768-G-A

20085933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16583794-G-T

20085974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16583828-C-T

http://identifiers.org/hco/10/GRCh38#20085983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16583838-A-C

20086694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16584467-C-T

20086695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16584468-C-T

20086801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16584568-G-A

20086844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16584605-C-G

20086844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16584605-C-T

20086869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16584619-T-C

20086873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16584625-A-G

20086874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16584626-C-T

http://identifiers.org/hco/10/GRCh38#20086998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16584710-A-C

20087064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16584777-A-T

20087343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16585044-G-T

20087409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16585081-A-T

20087447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16585119-T-A

20087487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16585161-C-T

20087489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16585163-A-G

http://identifiers.org/hco/10/GRCh38#20087590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16585259-C-A

20087590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16585259-C-T

20087648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16585320-A-T

20087878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16585534-A-T

20087893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16585549-G-A

20087924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16585570-T-C

20088040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16585687-A-G

20088199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16590996-T-C

20088209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16591006-A-T

20088374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16591171-G-A

20088383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16591877-C-T

20088425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16591923-A-G

20088442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16591941-A-G

20088442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16591941-A-T

20088591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16592057-G-A

20088688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16592156-C-T

20088980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16592449-C-G

20088980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16592449-C-T

20088987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16592456-C-G

20088987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16592456-C-T

20089003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16592472-C-G

20089140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16592585-C-G

20089257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16592690-C-G

20089653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16593219-G-T

20089829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16593376-T-C

20089864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16593401-G-A

20089937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16593447-C-G

20089937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16593447-C-T

20089943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16593453-C-G

20090138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16593625-C-T

20090216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16593700-A-G

20090252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16593736-T-C

20090332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16593832-A-G

20090360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16593859-G-A

20090360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16593859-G-T

20090415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16593910-A-G

20090508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16594002-C-G

20090742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16594226-A-G

http://identifiers.org/hco/10/GRCh38#20090849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16594300-A-C

20090849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16594300-A-G

20090993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16594863-A-T

20091175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16595032-T-A

http://identifiers.org/hco/10/GRCh38#20091248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16595077-A-C

http://identifiers.org/hco/10/GRCh38#20091353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16595168-C-A

20091379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16595191-C-T

20091512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16597849-C-T

20091523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16597860-G-C

20091594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16597925-T-C

20091639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16597990-A-G

20091711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598075-G-A

20091791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598150-A-G

20091857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598200-C-G

20091869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598212-A-G

20091869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598212-A-T

20091881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598224-G-T

20091929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598271-G-T

20091956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598298-A-G

20091978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598320-C-T

20092017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598356-C-T

20092103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598791-T-G

20092240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598909-T-A

20092240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598909-T-G

20092282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16598938-T-C

20092427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16599093-T-C

20092624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16599308-A-T

20096832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16600786-G-A

20097070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16601026-G-A

20097430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16601377-G-A

20097570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16601520-C-T

20097695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16601649-G-A

20097938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16601857-A-G

20098065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16601940-T-G

20098152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16602008-T-G

20098274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16602146-A-G

20098286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16602159-A-T

20098308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16602184-G-A

20098466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16602324-G-A

20098475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16602333-C-T

20098645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16602495-C-T

20098667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16602517-G-A

20099013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16602736-A-G

20099707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16604282-C-G

20099748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16604325-G-A

20100022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16604585-C-T

20100132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16604666-A-G

20100175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16604707-A-G

20100332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16604881-C-T

20100373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16604912-G-A

20100478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16605015-A-G

http://identifiers.org/hco/10/GRCh38#20100521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16605058-A-C

http://identifiers.org/hco/10/GRCh38#20100881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16605415-C-A

20100888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16605422-T-A

20101198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16605691-G-A

20104136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16607400-G-C

20104254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16607525-A-G

20104550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16607787-A-G

20104557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16607794-C-G

20104627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16607864-A-G

20105240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16608896-G-C

20105816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16609475-A-G

20105821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16609480-T-G

20105848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16609494-A-G

20105887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16609522-T-C

20106383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16610976-G-A

20109590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16612216-T-A

20109590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16612216-T-G

http://identifiers.org/hco/10/GRCh38#20109611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16612237-A-C

http://identifiers.org/hco/10/GRCh38#20109642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16612268-C-A

20109706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16612382-C-T

http://identifiers.org/hco/10/GRCh38#20109729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16612405-C-A

20109729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16612405-C-T

20109818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16612500-C-T

20109967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16612618-C-T

20110120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16612769-G-A

20110120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16612769-G-C

20110333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16612976-G-T

20110413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16613040-C-T

20110537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16613161-A-G

20110594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16613236-A-G

20110908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16613549-G-C

20110962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16613602-T-C

http://identifiers.org/hco/10/GRCh38#20111017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16613664-A-C

20111017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16613664-A-G

20111058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16613710-A-G

20111131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16613783-T-A

20111131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16613783-T-C

20111175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16613827-G-A

20111256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16613903-A-G

20111410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16614157-G-A

20111444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16614191-A-G

20111454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16614201-T-G

20111563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16614305-C-T

20111574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16614316-G-A

20111630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16614372-G-T

20112264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16616485-G-A

http://identifiers.org/hco/10/GRCh38#20112364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16616589-C-A

20116244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16619522-T-G

http://identifiers.org/hco/10/GRCh38#20116323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16619614-C-A

20116348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16619636-A-G

20116439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16619715-A-G

20116447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16619725-T-A

20116467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16619745-A-G

20116483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16619761-A-G

20116508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16619784-A-G

20116563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16619838-A-G

20116569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16619844-G-A

20116579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16619854-G-A

20117709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16621895-G-A

20117714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16621900-T-C

20117804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16621981-T-G

20117904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16622092-G-T

20117918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16622106-T-A

20117971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16622147-A-G

20117979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16622155-T-C

20117980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16622156-G-C

20135498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16635957-G-A

20135614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16636030-T-C

20135779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16636196-A-G

http://identifiers.org/hco/10/GRCh38#20135810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16636234-A-C

20135966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16636370-A-G

http://identifiers.org/hco/10/GRCh38#20136286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16636626-A-C

20136287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16636627-C-G

20136373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16636725-G-A

20136384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16636736-G-T

20136401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16636752-T-C

20136423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16636778-G-A

http://identifiers.org/hco/10/GRCh38#20136511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16636830-C-A

20136511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16636830-C-T

20136534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16636853-A-G

20136585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16636906-C-T

20136822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16637138-A-G

20136942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16637251-C-G

20136942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16637251-C-T

20137373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16637929-T-C

20138316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16638231-T-C

20139347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16639960-T-G

20139352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16639965-A-G

20139450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16640045-T-C

20140673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16640355-G-A

http://identifiers.org/hco/10/GRCh38#20140722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16640395-A-C

20140793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16640466-A-G

20140933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16640610-G-T

20141001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16640746-A-T

20141051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16640809-A-G

20141054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16640812-T-C

20141055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16640813-C-T

20141078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16640835-A-G

http://identifiers.org/hco/10/GRCh38#20141099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16640856-C-A

20141099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16640856-C-T

20141278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16640972-A-G

http://identifiers.org/hco/10/GRCh38#20141303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16640997-A-C

20141312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16641407-G-A

20141436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16641517-C-T

20141481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16641547-A-G

http://identifiers.org/hco/10/GRCh38#20141553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16641617-A-C

20141727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16641811-G-A

20141958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16641914-A-T

20142033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16641926-A-G

20142033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16641926-A-T

20142077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16641940-G-T

20142103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16641966-A-G

20142142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16642005-C-T

http://identifiers.org/hco/10/GRCh38#20142152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16642014-A-C

http://identifiers.org/hco/10/GRCh38#20142299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16642165-C-A

20142594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16642467-T-G

20142655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16642525-G-A

20142699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16642569-A-G

20142707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16642577-T-C

20142794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16642656-A-T

20142979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16643055-G-A

20143077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16643201-C-T

20143095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16643227-C-T

20143106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16643238-A-G

20143166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16643289-G-A

20143166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16643289-G-T

20143271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16643374-T-C

20143279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16643382-A-G

20143279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16643382-A-T

20143407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16643510-T-C

20143950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16646515-T-C

20143998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16646562-A-G

20145913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16650779-T-C

20146730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16651316-T-A

20146730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16651316-T-C

20147042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16652903-G-A

20147056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16652916-T-C

20147074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16652939-C-T

20147125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16652991-C-T

20147371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16653229-G-A

20147398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16653256-T-A

20147647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16654789-A-G

20147654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16654796-A-T

20147656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16654798-A-G

20147656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16654798-A-T

20147919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655055-T-A

20147919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655055-T-G

20148020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655133-T-C

20148022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655135-G-A

20148022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655135-G-T

20148064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655176-T-G

20148077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655196-T-C

20148077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655196-T-G

20148111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655228-G-C

20148121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655237-T-A

20148310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655390-C-T

20148348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655415-G-A

20148419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655476-G-A

20148458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655513-G-C

20148565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655616-T-G

20148568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655619-G-A

20148616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655667-T-G

20148745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655804-A-T

20148849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655981-C-T

20148858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16655990-A-T

20148882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16656014-A-T

20148935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16656060-T-C

20148979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16656111-T-G

20150506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16656251-C-T

20150597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16656361-G-A

20150831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16656610-G-T

20151021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16656804-T-A

20151076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16656879-C-G

20151078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16656881-C-T

20151097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16656926-C-T

20151249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16657374-A-G

20151362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16657480-T-C

20151612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16657715-C-T

http://identifiers.org/hco/10/GRCh38#20151742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16657841-A-C

20151776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16657874-T-A

20151793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16657891-G-A

20151822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16657920-G-C

20151890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16657988-T-C

20152032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16658094-A-G

20152096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16658180-T-C

http://identifiers.org/hco/10/GRCh38#20152150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16658233-A-C

20152404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16658485-G-C

20152431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16658512-G-T

20152457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16658542-G-C

20152457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16658542-G-T

20154649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16659281-C-T

20154782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16659389-G-A

20155149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16659711-A-T

20155322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16659869-G-A

20155372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16659917-T-G

20155386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16659931-A-G

20155423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16659970-A-G

20155447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16660100-T-C

20155506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16660162-G-T

http://identifiers.org/hco/10/GRCh38#20155601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16660313-A-C

20155601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16660313-A-G

20155713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16660411-G-T

20155988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16660770-T-A

http://identifiers.org/hco/10/GRCh38#20156006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16660794-A-C

20156008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16660796-G-T

20156195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16660955-T-G

http://identifiers.org/hco/10/GRCh38#20156261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#16661023-A-C

20156294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16661057-T-C

20156302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16661065-A-G