49710346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95272687-A-G

http://identifiers.org/hco/17/GRCh38#49710647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95272327-C-A

49710647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95272327-C-G

49710647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95272327-C-T

49710648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95272326-G-A

49710648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95272326-G-T

49710758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95272232-G-A

49710758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95272232-G-T

49710955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95272066-A-G

http://identifiers.org/hco/17/GRCh38#49711207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95271833-C-A

49711207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95271833-C-T

49711384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 95271657-C-G

49711384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 95271657-C-T

49711584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95271460-A-T

49711660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95271355-G-T

49715531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95270440-C-T

49716029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95269964-G-T

49716113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95269865-A-G

49716113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95269865-A-T

49716510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95269436-C-G

http://identifiers.org/hco/17/GRCh38#49716554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95269396-A-C

49717018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95268954-T-G

49717106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95268867-T-C

http://identifiers.org/hco/17/GRCh38#49717479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95268538-A-C

49717605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, start_lost
orthologous variants: 95268413-A-G

49717760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95268264-G-T

49717777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95268247-G-A

49717777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95268247-G-C

http://identifiers.org/hco/17/GRCh38#49717864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95268179-C-A

49717864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95268179-C-T

http://identifiers.org/hco/17/GRCh38#49717873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95268171-C-A

49717932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95268119-T-G

49718046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 95268045-T-C

49718070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95268023-T-C

49718130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95267962-A-T

49718228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95267867-A-G

49718308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95267431-G-A

49718601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95267545-G-A

49718660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95267498-G-A

http://identifiers.org/hco/17/GRCh38#49718668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95267490-C-A

49718836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95267323-G-A

49719217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95267064-C-T

http://identifiers.org/hco/17/GRCh38#49719484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95266813-C-A

49719484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95266813-C-T

http://identifiers.org/hco/17/GRCh38#49719500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95266797-C-A

49719500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95266797-C-T

http://identifiers.org/hco/17/GRCh38#49719519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95266788-C-A

49719519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95266788-C-T

49719601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95266733-T-A

49719601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95266733-T-C

49719641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95266694-T-G

49719681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95266654-A-G

http://identifiers.org/hco/17/GRCh38#49719690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95266645-C-A

49719690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95266645-C-T

49719696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95266639-T-A

49719717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95266618-A-G

http://identifiers.org/hco/17/GRCh38#49719735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95266610-C-A

49719735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95266610-C-G

49719735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95266610-C-T

http://identifiers.org/hco/17/GRCh38#49719848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95266499-C-A

49719860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95266487-A-T

49719969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95266374-A-G

49719969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95266374-A-T

49720014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95266214-T-C

49720151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266081-A-T

49720181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266054-G-A

49720181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266054-G-T

49720464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95265782-G-T

49720466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95265780-C-T

http://identifiers.org/hco/17/GRCh38#49720496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95265750-C-A

49720496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95265750-C-G

http://identifiers.org/hco/17/GRCh38#49720498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95265748-C-A

49720498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95265748-C-G

49720512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95265736-G-T

49720554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95265701-G-T

49721507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95263205-T-C

49721554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95263158-T-C

49722278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262744-C-T

49722363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262663-A-G

49722572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95262284-A-G

49722604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262252-G-T

http://identifiers.org/hco/17/GRCh38#49722626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95262229-A-C

49722635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262220-G-T

49722654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262208-G-A

49722654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262208-G-T

49722658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262204-A-G

49722719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262140-A-G

49722871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261993-T-C

49722895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261878-G-A

49722991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261632-G-T

49722992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261631-T-A

49723021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261607-T-C

49723292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261374-T-C

49723513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261179-G-A

49723516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261178-C-T

http://identifiers.org/hco/17/GRCh38#49723902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95260825-A-C

49724089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95260673-C-T

49724166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95260611-A-T

49724201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95260572-C-T

49724945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95260195-G-A

49724945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95260195-G-C

49727762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95259263-A-T

http://identifiers.org/hco/17/GRCh38#49728724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95258281-A-C

49729016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95257743-G-C

http://identifiers.org/hco/17/GRCh38#49729429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95257358-C-A

49730237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95256711-G-A

49731172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95255842-T-C

49731619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95255432-G-A

49731634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95255417-G-A

http://identifiers.org/hco/17/GRCh38#49731664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95255392-A-C

49732463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95255050-C-T

49732734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95254809-C-G

49732734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95254809-C-T

http://identifiers.org/hco/17/GRCh38#49732766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95254776-A-C

49732766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95254776-A-T

49732790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95254750-C-G

49732790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95254750-C-T

49732974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254595-T-C

49733001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254574-T-A

49733001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254574-T-C

49733001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254574-T-G

49733136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254440-C-T

49733630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254030-A-G

49733843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95253822-T-C

http://identifiers.org/hco/17/GRCh38#49734436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95253634-A-C

49734570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 95253595-C-T

49734612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 95253561-T-A

49735012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95253318-A-G

49735465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95252772-T-C

49735507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95252733-T-C

49735852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95252432-T-G

49736010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95252263-C-T

49736766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95250999-C-T

http://identifiers.org/hco/17/GRCh38#49737353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95250432-A-C

49738280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249564-C-G

49738478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249386-T-C

http://identifiers.org/hco/17/GRCh38#49738742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95249138-C-A

49738742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249138-C-G

49739064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95248818-G-A

49739095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95248763-G-A

49739396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95248218-G-C

49739459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95248081-G-A

49740104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95247479-G-A

49740153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95247446-C-T

http://identifiers.org/hco/17/GRCh38#49740707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95247235-C-A

49741119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95246895-G-A

49741455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95246636-T-A

49741466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95246623-G-A

49741786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95246390-C-T

http://identifiers.org/hco/17/GRCh38#49741946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95246174-A-C

49742144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95245907-G-A

49742206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95245844-T-C

49743221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95244862-A-G

49745333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95244257-C-T

49745417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95244170-A-T

49747719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95241500-T-C

49747999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95241241-A-G

49748504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95240739-G-A

49748686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95240554-A-G

49749158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95239768-G-A

49749612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239459-A-G

49749612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239459-A-T

49749613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239458-G-A

http://identifiers.org/hco/17/GRCh38#49749787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95239286-C-A

49749829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239244-G-C

49749829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239244-G-T

49750177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95238964-G-A

49752350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237411-C-T

49752351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237410-T-G

49752356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237405-C-T

49752607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237172-C-T

49752822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95236941-T-C

http://identifiers.org/hco/17/GRCh38#49754118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95236328-C-A

49754118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95236328-C-G

49754118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95236328-C-T

49754141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95236305-T-G

http://identifiers.org/hco/17/GRCh38#49754202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95236244-A-C

49754211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95236236-C-T

49754692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95236050-T-G

49755324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95235761-G-A

49755570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95235518-C-T

49755775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95235321-C-T

49755979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95235124-C-T

49757007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95234484-C-T

49757212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95234289-G-A

49757410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95234094-G-A

49757410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95234094-G-T

49757660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95233883-G-A

49757660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95233883-G-C

http://identifiers.org/hco/17/GRCh38#49758694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95233150-C-A

49758778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95233049-A-G

49758991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95232786-T-A

http://identifiers.org/hco/17/GRCh38#49759005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95232772-C-A

49759796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95232004-C-T

49759799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95232001-C-T

49760039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95231783-G-A

49760119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95231702-T-C

49760680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95231124-C-T

49760928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95230858-C-G

http://identifiers.org/hco/17/GRCh38#49761065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95230724-C-A

49761161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95230631-G-C

49761574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95230247-A-G

http://identifiers.org/hco/17/GRCh38#49761713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95230111-A-C

49761713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95230111-A-G

49762132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95229714-C-T

49762139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95229696-T-C

49762312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95229519-A-G

49762668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95229195-A-G

http://identifiers.org/hco/17/GRCh38#49763678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95228255-C-A

49763678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228255-C-G

http://identifiers.org/hco/17/GRCh38#49763768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95228167-C-A

49763768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228167-C-G

49763791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228142-T-A

49763791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228142-T-C

49763791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228142-T-G

49763867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228110-G-A

49763867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228110-G-C

49763867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228110-G-T

http://identifiers.org/hco/17/GRCh38#49764311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95227665-C-A

49764311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95227665-C-T

49764325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95227638-C-T

http://identifiers.org/hco/17/GRCh38#49765441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95226568-C-A

49765445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95226564-C-T

49765461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95226557-A-T

49765619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95226404-T-G

49765698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95226329-G-A

49765698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95226329-G-T

http://identifiers.org/hco/17/GRCh38#49766025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95226017-A-C

49766084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95225959-T-C

49766199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95225852-C-T

49766204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95225847-G-C

49766420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95225658-C-T

49766637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95225470-C-T

49767337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95224614-C-T

49767419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95224536-G-A

49767503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95224269-C-G

49767503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95224269-C-T

49768008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95223429-T-C

49768032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95223405-G-C

49771701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95219704-T-G

49771787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95219631-A-G

49772935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95219247-G-A

49772953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95219223-C-T

49772954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95219222-G-A

49772954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95219222-G-C

49773016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95219125-C-T

49773039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95219102-C-G

49773061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95219080-T-C

49773079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95219063-G-A

http://identifiers.org/hco/17/GRCh38#49773576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95218587-C-A

49773578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95218585-T-C

49773601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95218562-C-T

49775500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217445-C-G

49775736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217281-G-A

49775857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217161-C-G

49775921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217099-T-C

http://identifiers.org/hco/17/GRCh38#49776397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95216669-C-A

49776397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95216669-C-T

49776673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95216393-G-C

49776777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95216285-A-G

49776866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95216196-G-A

49776866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95216196-G-T

49777045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95215900-A-G

49777083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95215862-G-C

49777170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95215785-G-C

49777400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95215556-G-A

49777579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95215408-G-A

49777615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95215370-C-T

49777875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95215111-T-C

49778326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95214641-C-T

49779331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95211182-A-G

49779726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95210828-T-G

49780671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95209056-T-C

49780696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95209031-A-G

49780766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95208966-T-G

49780830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95208902-C-T

49780878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95208844-T-C

49782992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95206818-C-G

49783497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95206288-G-A

49783502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95206283-T-C

49783611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95206171-G-A

49783662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95205673-C-T

http://identifiers.org/hco/17/GRCh38#49783868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95205455-A-C

49784002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95205337-C-T

49784242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95204263-A-G

49784298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95204215-T-C

49784304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95204209-T-G

49784306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95204207-G-A

49784415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95204105-T-G

49784717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95203820-C-G

49784778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95203757-T-C

49785309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95203363-C-T

49785767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95203005-T-C

49785798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95202974-T-A

49785798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95202974-T-G

49787164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95202794-T-G

49787255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95202706-C-T

49787928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95201781-A-G

49788138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95201575-G-C

49788276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95201437-T-C

49788318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95201395-C-T

http://identifiers.org/hco/17/GRCh38#49788382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#95201337-C-A

49788382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95201337-C-T

49788490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 95201219-C-T

http://identifiers.org/hco/17/GRCh38#49788566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#95201143-C-A

49788566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95201143-C-T

49788673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95201036-G-A

49788704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95201005-G-A

49788716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95200993-T-C

49788716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95200993-T-G

49788793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95200915-G-A

49788793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95200915-G-T

49788870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95200838-G-A

49788870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95200838-G-C

http://identifiers.org/hco/17/GRCh38#49788912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#95200796-A-C

49788912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95200796-A-G

http://identifiers.org/hco/17/GRCh38#49788926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#95200782-C-A

49788974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95200734-A-T

49788979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95200729-C-T

http://identifiers.org/hco/17/GRCh38#49789122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24179
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#95200586-C-A