24698379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50184405-G-T

24698427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50184459-G-A

24698477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50184509-T-A

24698477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50184509-T-C

24698495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50184527-T-C

http://identifiers.org/hco/7/GRCh38#24698540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50184559-A-C

24698540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50184559-A-G

24698660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50184665-T-C

24698684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50184693-T-C

24698778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50184748-C-T

24698821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50184764-A-G

http://identifiers.org/hco/7/GRCh38#24698836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50184778-C-A

24698873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50184806-A-G

24698956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50184868-G-T

24699220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50185147-C-T

24699308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50185228-T-G

24701141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50191971-G-A

24701141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50191971-G-T

24701453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50192273-G-A

24701706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50192477-C-G

24701737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50192504-C-T

24702228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50192895-A-G

24702394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50193048-A-G

24702430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50193079-T-G

http://identifiers.org/hco/7/GRCh38#24702488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50193121-A-C

24702644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50193233-T-G

24702737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 50193308-G-A

24702772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 50193342-T-C

24702772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 50193342-T-G

http://identifiers.org/hco/7/GRCh38#24702902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50193581-A-C

24702902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50193581-A-G

24702902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50193581-A-T

24702996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50193724-G-A

24702996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50193724-G-T

24703026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50193754-G-T

24703027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50193755-G-A

http://identifiers.org/hco/7/GRCh38#24703066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50193823-C-A

24703066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50193823-C-T

24703385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194196-A-G

24703601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194333-G-T

24703674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194378-T-C

24703686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194391-C-T

24703755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194433-G-A

24703755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194433-G-T

24703781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194460-G-T

24703794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194475-G-T

24703816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194502-G-T

http://identifiers.org/hco/7/GRCh38#24703863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50194549-A-C

24703863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194549-A-T

24703887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194574-C-T

24703924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194606-T-C

http://identifiers.org/hco/7/GRCh38#24703940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50194617-C-A

24704064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194678-A-G

24704067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194681-G-T

http://identifiers.org/hco/7/GRCh38#24704230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50194794-C-A

24704230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194794-C-T

24704280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194827-C-T

http://identifiers.org/hco/7/GRCh38#24704319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50194863-C-A

http://identifiers.org/hco/7/GRCh38#24704373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50194909-C-A

24704373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194909-C-T

24704390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50194926-A-G

24704540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195016-G-A

24704540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195016-G-T

http://identifiers.org/hco/7/GRCh38#24705007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50195242-C-A

24705007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195242-C-G

24705007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195242-C-T

24705291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195477-C-G

24705315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195498-G-T

http://identifiers.org/hco/7/GRCh38#24705485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50195658-C-A

24705485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195658-C-T

http://identifiers.org/hco/7/GRCh38#24705512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50195662-C-A

http://identifiers.org/hco/7/GRCh38#24705546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50195695-C-A

24705546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195695-C-T

24705564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195722-A-T

24705653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195780-A-G

24705658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195784-T-C

24705659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195785-G-A

24705736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195825-G-A

24705736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195825-G-T

http://identifiers.org/hco/7/GRCh38#24705737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50195826-C-A

24705737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195826-C-T

24705807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195884-G-C

24705807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195884-G-T

24705835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195913-G-C

http://identifiers.org/hco/7/GRCh38#24705842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50195920-C-A

24705842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195920-C-T

24705903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195967-G-A

24705953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195999-G-A

24705953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50195999-G-T

24705954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50196000-G-A

24705954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50196000-G-C

24705954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50196000-G-T

http://identifiers.org/hco/7/GRCh38#24705955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50196001-C-A

24705955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50196001-C-T

24705968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50196012-T-A

24705968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50196012-T-C

24705968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50196012-T-G

http://identifiers.org/hco/7/GRCh38#24706037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50196073-C-A

24706037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50196073-C-T

24706042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196078-T-A

24706042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196078-T-C

http://identifiers.org/hco/7/GRCh38#24706049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50196083-C-A

24706049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196083-C-G

24706062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196096-G-T

24706086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196116-T-A

24706097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196127-C-T

24706132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196161-A-T

24706157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196187-A-G

24706157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196187-A-T

24706245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: synonymous variant
orthologous variants: 50196281-G-A

24706245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: synonymous variant
orthologous variants: 50196281-G-C

24706278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: synonymous variant
orthologous variants: 50196314-C-T

24706315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: missense variant
orthologous variants: 50196351-C-T

24706317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: synonymous variant
orthologous variants: 50196353-G-A

http://identifiers.org/hco/7/GRCh38#24706424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50196478-C-A

24706424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196478-C-T

24706477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196536-T-C

24706590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196654-G-A

24706720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196793-T-C

http://identifiers.org/hco/7/GRCh38#24706724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50196797-A-C

24706724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196797-A-G

24706741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196814-C-T

24706747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196820-C-T

24706809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50196876-G-A

http://identifiers.org/hco/7/GRCh38#24707134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50197137-A-C

24707155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50197153-G-A

24707155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50197153-G-T

24707157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50197155-A-G

24707717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50197609-G-A

24707717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50197609-G-T

24707749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50197620-A-G

24707749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50197620-A-T

24707766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50197638-G-C

24707766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50197638-G-T

http://identifiers.org/hco/7/GRCh38#24707910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50197774-C-A

24707910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50197774-C-G

24707939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50197801-A-T

24708081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50197919-A-G

24708092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50197930-G-A

24708092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50197930-G-T

24708226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50198068-A-T

24708297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50198130-C-T

24708383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50198186-T-A

http://identifiers.org/hco/7/GRCh38#24708775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50198512-A-C

24708775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50198512-A-G

http://identifiers.org/hco/7/GRCh38#24708814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50198549-C-A

24709012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50198696-C-G

24709210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50198891-G-A

24709508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50199151-G-C

24709623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50199231-C-T

http://identifiers.org/hco/7/GRCh38#24709828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50199429-C-A

24709882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50199489-G-A

24709994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50199588-G-A

24709996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50199590-C-T

24710198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50199698-C-G

24710199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50199699-A-G

24710227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50199719-G-C

24710280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50199772-G-C

24710354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 50199846-G-A

http://identifiers.org/hco/7/GRCh38#24717351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50204356-A-C

http://identifiers.org/hco/7/GRCh38#24717511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50204482-C-A

24717511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50204482-C-G

24717511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50204482-C-T

24717527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50204498-T-C

24717865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50205337-G-C

24718125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50205549-G-A

24718153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50205576-C-T

24718361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50205737-A-G

http://identifiers.org/hco/7/GRCh38#24718917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50206163-C-A

24718917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50206163-C-G

24718917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50206163-C-T

24718925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50206171-G-C

24718925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50206171-G-T

24718933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50206180-G-T

24718940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50206187-T-A

24718940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50206187-T-C

http://identifiers.org/hco/7/GRCh38#24718942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50206189-C-A

24718942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50206189-C-G

24718942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50206189-C-T

24718996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50206242-G-A

24718996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50206242-G-C

24718996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50206242-G-T

http://identifiers.org/hco/7/GRCh38#24719012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#50206254-C-A

24719012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50206254-C-T

24719073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 50206292-C-T

24719146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 50206365-T-C

24719191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 50206410-G-C

24719238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50206457-G-A

24719238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50206457-G-T

24719258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50206477-G-T

24719531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50206662-A-G

24719923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50206812-G-A

24719933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50206825-G-C

24719994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50206879-A-G

24720442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50207281-C-T

24721688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50208195-A-G

24721688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50208195-A-T

24721757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50208265-T-C

24721776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50208284-C-G

24721776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50208284-C-T

24721832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50208342-C-G

24721832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50208342-C-T

24721915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50208423-C-T

24721999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50208507-G-T

24722114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50208624-C-T

24722248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50208756-C-T

24722392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50213609-C-T

24722434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50213651-A-G

http://identifiers.org/hco/7/GRCh38#24722445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50213662-C-A

24722613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50213813-C-T

24722638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50213837-C-T

24727066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50214322-C-T

24727080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50214336-G-C

24727180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50214432-G-T

24727451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50214890-T-C

24727517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50214967-T-C

24727586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50215036-C-T

24727744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50215183-T-C

24727895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50215325-C-T

24728042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50215440-G-T

24728071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50215470-T-C

24728074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50215473-G-A

24728080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50215479-C-T

24728284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50215677-C-T

24728299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50215698-A-G

24728839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50216546-C-G

24729239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50217784-T-C

24729306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50217851-G-C

24729385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50217929-A-G

http://identifiers.org/hco/7/GRCh38#24729485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50218013-C-A

24729518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50218044-C-G

24729557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50218097-C-T

24729641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50218158-G-A

24729742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50218269-G-C

24729742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50218269-G-T

24729851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50218376-G-C

24730045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50218512-G-A

24730221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50218695-G-A

24730225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50218699-C-T

24730243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50218717-T-C

24740753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50220136-G-A

24740775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50220152-T-G

24740926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50220298-G-A

http://identifiers.org/hco/7/GRCh38#24740973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50220373-C-A

24741100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50220463-T-C

24741117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50220480-A-T

24741335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50220693-T-C

24741421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50220780-T-C

http://identifiers.org/hco/7/GRCh38#24741522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#50220885-A-C

24742619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50222157-T-C

24742766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50222324-C-G

24744690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 50223038-C-T

http://identifiers.org/hco/7/GRCh38#24744697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50223045-C-A

24744726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 50223074-G-A

24744726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 50223074-G-C

24744789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50223133-A-G

24744811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50223156-T-G

24746761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50224836-G-C

24749560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50228252-A-G

24749838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50228527-T-A

24749838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50228527-T-C

24749977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50228692-A-G

24750961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50230374-A-G

24751411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50231820-T-C

24751836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50232158-G-A

http://identifiers.org/hco/7/GRCh38#24752273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50232684-A-C

24752494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50233080-T-C

24752498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50233084-A-G

24752498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50233084-A-T

24752511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50233097-T-C

24752511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50233097-T-G

24752593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50233206-G-C

24752593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50233206-G-T

24752852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50233495-T-C

http://identifiers.org/hco/7/GRCh38#24752864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50233508-C-A

http://identifiers.org/hco/7/GRCh38#24752955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50233594-C-A

24752955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50233594-C-T

24753289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50233910-C-T

24753312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50233934-T-C

24753409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50234068-C-G

24753422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50234081-C-T

24753537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50234333-A-T

24753539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50234335-A-G

24753540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50234336-T-C

24753552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50234347-T-A

24753552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50234347-T-C

24753553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50234348-G-A

24754142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50235962-T-A

24754551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50236053-T-C

http://identifiers.org/hco/7/GRCh38#24754566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50236068-C-A

24754919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50236491-A-G

24755366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50236939-T-C

http://identifiers.org/hco/7/GRCh38#24755652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50237157-A-C

24755653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50237158-G-C

http://identifiers.org/hco/7/GRCh38#24755702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50237198-C-A

24755806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50237293-G-A

24755881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50237367-G-A

24756152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50237414-G-A

24756161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50237423-G-A

24756210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50237468-A-G

24756985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 50238333-C-G

http://identifiers.org/hco/7/GRCh38#24757181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50238536-A-C

24757245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant
orthologous variants: 50238581-C-G

24757246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 50238582-T-C

24757246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 50238582-T-G

24757256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant
orthologous variants: 50238592-A-G

24757268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant
orthologous variants: 50238604-A-G

24757279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 50238617-G-A

24757279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 50238617-G-T

24757284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant
orthologous variants: 50238622-A-G

24757313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant
orthologous variants: 50238641-G-A

24757313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant
orthologous variants: 50238641-G-T

http://identifiers.org/hco/7/GRCh38#24757325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50238652-C-A

24757346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant
orthologous variants: 50238666-G-A

24757346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant
orthologous variants: 50238666-G-C

24757346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant
orthologous variants: 50238666-G-T

http://identifiers.org/hco/7/GRCh38#24757362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#50238681-C-A

24757362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, missense_variant
orthologous variants: 50238681-C-T

24757411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 50238722-T-G

24757424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 50238735-G-A

24757424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 50238735-G-T

24757454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 50238761-G-T

24757495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 50238789-G-A

24757495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 50238789-G-T

24757561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 50238862-C-T

24759441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50241303-G-C

24759490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50241343-T-C

24759515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50241371-A-G

24759679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50241473-T-C

24759866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50241574-A-G

24762309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2810
most severe consequence: intron variant
orthologous variants: 50242459-T-G