http://identifiers.org/hco/3/GRCh38#172039993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#27765048-C-A

172040155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27764955-C-G

172040155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27764955-C-T

172040269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27764842-G-A

172040278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27764833-C-G

172040278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27764833-C-T

172040284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27764827-T-G

172041011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27764092-G-A

172041638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27763595-A-G

172041638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27763595-A-T

172041796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27763434-T-A

172041960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27763277-G-T

172042053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27763184-G-A

172042088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27763152-T-A

172042244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27763000-G-A

172042244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27763000-G-T

172042417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27762857-A-G

172042418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27762856-G-C

172042689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27762544-C-T

172042784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27762470-A-T

172042835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27762419-T-G

http://identifiers.org/hco/3/GRCh38#172044153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27761291-C-A

172044153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27761291-C-T

172044370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27760344-A-G

172045317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27759477-T-C

172045371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27759424-G-C

172045491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27759300-T-C

172045539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27759257-G-T

172045753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27759121-T-C

172045841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27759048-G-A

http://identifiers.org/hco/3/GRCh38#172046162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27758746-A-C

http://identifiers.org/hco/3/GRCh38#172046301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27758635-A-C

172046301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27758635-A-T

172046312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27758624-A-G

172046732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27758473-A-T

172046787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27758417-A-G

172046851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27758363-G-T

http://identifiers.org/hco/3/GRCh38#172046955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27758210-C-A

172046955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 27758210-C-G

http://identifiers.org/hco/3/GRCh38#172047106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27758043-C-A

172050751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27754478-C-G

172050751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27754478-C-T

172050797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27754432-A-G

172050988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27754265-T-C

172051069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27754189-T-C

172053949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27753032-T-C

172054039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27752945-T-C

172054845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27752278-T-G

http://identifiers.org/hco/3/GRCh38#172054927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27752204-A-C

172055089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27751593-T-C

172055500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27751186-A-T

172056230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27750600-G-A

172056230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27750600-G-T

172056874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27749958-T-C

172056881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27749953-C-T

172057135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27749692-G-A

172057245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27749584-G-A

172057245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27749584-G-C

http://identifiers.org/hco/3/GRCh38#172057476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27749171-A-C

172057712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27748940-T-A

172057745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27748908-A-T

172057914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27748739-A-T

172058014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27748637-T-G

172058165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27748404-C-T

172058294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27748115-C-T

172058778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27747727-T-C

172058859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27747646-T-C

172059025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27747474-A-G

172059614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27746963-G-A

172059614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27746963-G-C

172059614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27746963-G-T

172059628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27746949-G-T

172059660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27746917-C-T

172059664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27746912-T-A

172059744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27746833-T-G

172060093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27746521-A-G

172060191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27746430-C-T

172060595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27745749-A-G

http://identifiers.org/hco/3/GRCh38#172060843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27745501-A-C

172061031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27745301-G-A

172061031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27745301-G-T

172061544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27744748-G-C

172061605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27744676-T-C

172061689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27744598-A-G

172062031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27744284-G-A

http://identifiers.org/hco/3/GRCh38#172062188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27744165-C-A

172062468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27743913-C-T

172062766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27743752-C-T

172062984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27743568-T-G

172064396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27742411-C-T

172064643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27742174-A-G

172065988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27740821-A-G

172066076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27740744-C-T

172066368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27740234-C-T

172066499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27740117-T-A

172067158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27739490-C-T

172067334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27739339-T-G

172067569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27739147-A-G

172067576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27739140-G-A

http://identifiers.org/hco/3/GRCh38#172067967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27738795-A-C

172068047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27738707-G-A

172068168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27738278-C-G

172068244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27738191-A-T

172068315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27738110-C-T

172068325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27738096-A-G

172068406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27738019-G-A

172068744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27737968-G-T

172068822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27737892-A-G

172069019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27737727-T-C

172069061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27737686-T-C

172069188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27737572-G-A

172069252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27737501-C-T

172069286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27737475-A-G

172069453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27737160-G-A

172069678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27736937-G-A

172070022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27736642-G-A

172070234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27736468-C-T

172070381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27736254-G-C

172070381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27736254-G-T

172070382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27736253-T-G

http://identifiers.org/hco/3/GRCh38#172070488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27736154-C-A

172070499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27736143-T-C

172070508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27736134-T-A

172072358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27734364-A-G

172072565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27734159-C-T

172072848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27733862-A-G

172073042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27733682-G-A

172073065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27733667-A-G

172074464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27732258-A-G

172075781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27729905-A-T

172076019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27729690-T-C

http://identifiers.org/hco/3/GRCh38#172076054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27729660-A-C

172076189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27729547-G-A

172076189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27729547-G-T

http://identifiers.org/hco/3/GRCh38#172076308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27729450-A-C

172076308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27729450-A-G

172076493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27729295-G-A

172076843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27729020-G-T

172077020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27728873-A-G

172077040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27728852-A-T

http://identifiers.org/hco/3/GRCh38#172078926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27727915-C-A

172078926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27727915-C-T

http://identifiers.org/hco/3/GRCh38#172078930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27727911-C-A

172079237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27727660-G-A

172079306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27727551-G-A

172079825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27727097-G-A

172080122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27726928-A-G

172080707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27726684-C-T

172081022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27726387-G-A

http://identifiers.org/hco/3/GRCh38#172081613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27725679-C-A

172081621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27725671-T-C

172081695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27725580-T-C

172082258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27725016-G-A

172082365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27724909-A-G

172082491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27724783-A-G

172082565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27724708-A-G

172082623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27724651-T-C

172082658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27724617-A-G

172082861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27724410-T-A

172083041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27724226-G-C

172083041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27724226-G-T

172083288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27724032-C-T

172083386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27723935-T-A

172083665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27723737-A-G

172083764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27723635-A-G

172084836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27722394-A-G

172084873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27722357-T-C

172085218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27722074-T-C

172085411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27721964-C-T

172085596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27721796-C-T

172085655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27721738-T-G

172087110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27720486-G-A

172087260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27720355-G-A

172087357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27720283-G-T

172087481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27720178-G-A

172087481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27720178-G-C

172087506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27720150-A-G

172087788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27719899-G-A

172088346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27719415-A-T

172088862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27719126-G-A

172089177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27718874-T-G

172089197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27718854-T-C

172089198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27718853-A-T

172089278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27718769-T-C

172089315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27718740-G-A

172089438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27718610-G-A

172089851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27718318-A-T

172090524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27717470-T-G

172090543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27717451-G-A

172090689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27717338-G-A

172091751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27716541-T-G

172094779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27716092-T-C

172094812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27716077-G-A

172094929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27715958-T-C

172094932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27715955-A-G

172095244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27715659-A-G

http://identifiers.org/hco/3/GRCh38#172095361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#27715545-A-C

172096051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27712702-C-G

172096051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27712702-C-T

172096056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27712697-A-G

172096422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27712383-C-G

172096820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27711533-A-G

172096892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27711465-G-C

172096900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27711457-G-T

172097316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27711058-T-C

172097618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27710770-T-C

172097618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27710770-T-G

http://identifiers.org/hco/3/GRCh38#172097697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27710699-A-C

172097743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27710656-C-G

172097743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27710656-C-T

172099329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27709516-A-G

172101902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27707985-A-T

172101903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27707984-A-G

172102174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27707724-T-C

172102242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27707667-A-G

172102388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27707566-T-A

172102405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27707552-T-C

http://identifiers.org/hco/3/GRCh38#172102599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27707357-A-C

172102599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27707357-A-T

172102834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27707187-C-G

172102926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27707080-C-T

172103035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27706966-G-A

172103035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27706966-G-C

172103137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27706864-G-A

172103150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27706851-G-A

172103150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27706851-G-T

172103288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27706733-T-C

172103330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27706692-G-T

172103611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27706379-G-A

172103611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27706379-G-T

172103967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27706020-A-G

http://identifiers.org/hco/3/GRCh38#172104129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27705863-A-C

172104390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27705598-T-G

172104406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27705582-T-G

172104418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27705570-C-G

172104418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27705570-C-T

172104459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27705496-A-G

172104579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27705338-A-G

172105201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27704324-G-A

172105237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27704299-T-C

172105362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27704179-A-G

172105393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27704142-C-T

172105449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27704096-T-C

172105733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27703426-A-G

172105889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27703329-T-A

172105922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27703296-T-C

172106120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27703096-A-G

172106592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27702624-G-A

172106595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27702621-A-G

172107076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27702175-A-G

http://identifiers.org/hco/3/GRCh38#172107280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27701974-A-C

172107424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27701937-G-C

172107496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27701880-A-T

172108945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27701040-T-C

172108954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27701035-C-T

172108973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27701016-G-T

172109075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27700915-G-C

172110074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27700679-G-T

172110293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27700462-T-G

172110359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27700397-T-A

172110359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27700397-T-C

172110456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27700301-G-A

172110607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27700189-C-T

172111157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27699318-A-G

172111179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27699298-G-T

172111240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27699241-G-C

172111422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27699083-C-T

172111423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27699082-G-A

172111469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27699037-A-G

172111499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27699012-T-A

172111501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27699010-G-C

172111627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27698883-G-C

172111689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27698824-A-G

172111971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27698577-T-C

172111979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27698565-T-C

172112301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27697389-C-G

http://identifiers.org/hco/3/GRCh38#172112311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27697379-C-A

http://identifiers.org/hco/3/GRCh38#172112341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27697345-A-C

172112341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27697345-A-T

172112596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27697092-T-G

172112627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27697078-C-G

172112629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27697076-A-G

172112730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27696985-T-C

http://identifiers.org/hco/3/GRCh38#172113096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27696681-A-C

172113146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27696631-G-A

172113177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27696600-G-A

172113348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27696442-A-G

172113427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27696364-C-T

172113832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27695822-C-G

172113889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27695762-G-A

172113931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27695720-C-T

172113998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27695629-C-G

172114001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27695626-C-G

172114010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27695603-C-T

172114066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27695517-G-C

172114093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27695436-C-G

172114136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27695390-G-A

172114295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27695245-C-T

172114491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27695081-C-T

172115139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27694041-C-G

172115143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27694037-C-T

172117736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27693584-T-C

172117755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27693566-G-A

172117912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27693389-G-A

172118445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27692853-A-G

172118814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27692560-A-G

172118816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27692558-A-T

http://identifiers.org/hco/3/GRCh38#172119861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27691636-C-A

http://identifiers.org/hco/3/GRCh38#172119863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27691634-C-A

172119863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27691634-C-G

172119943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27691559-T-C

172120023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27691488-C-G

172120438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27691114-G-C

172122188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27689170-A-G

172122188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27689170-A-T

172122257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27689101-C-T

172122260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27689098-A-G

172122261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27689097-A-G

172122273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27689085-A-G

172122349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27689022-T-C

172122556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27688855-A-G

172122556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27688855-A-T

172122760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27688705-T-C

172124890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27687379-T-A

172124890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27687379-T-C

172124958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27687308-A-G

172125090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27687188-A-T

172125133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27687159-T-C

172125387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27686508-T-G

172125508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27686439-G-A

172125508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27686439-G-T

172125509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27686438-T-G

172125590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27686364-A-G

172125598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27686356-A-G

http://identifiers.org/hco/3/GRCh38#172125792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27685935-C-A

172126312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27685415-T-A

172126363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27685364-A-G

172126368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27685359-T-A

172126373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27685354-A-G

172126918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27684107-T-C

172126926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27684099-A-G

172126955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27684075-C-T

172126970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27684060-G-A

172126970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27684060-G-T

172127004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27684027-G-T

172127049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27683991-T-C

172127062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27683977-G-T

172127090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27683949-A-G

172127416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27682839-C-T

172127521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27682719-G-C

172127647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27682618-T-C

172127647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27682618-T-G

172127662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27682613-A-G

172128284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27681930-T-C

172128545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27681679-A-T

172128769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27681063-A-G

172128790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27681043-T-C

172128926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27680905-C-G

172128926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27680905-C-T

172128979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27680853-T-C

172129331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27680326-T-A

172129549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27680140-A-T

172129835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679844-G-A

172129835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679844-G-T

172129840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679839-G-A

172129933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679724-G-A

172130079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679588-C-T

172130088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679579-C-T

172130391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27679273-A-G

172130928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27677660-G-A

http://identifiers.org/hco/3/GRCh38#172131393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27676703-C-A

172131487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27676617-T-C

172131509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27676594-A-G

172131628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27676473-A-G

172132866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27675341-T-A

http://identifiers.org/hco/3/GRCh38#172133270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27674985-A-C

172133272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674983-G-C

172133274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674981-G-A

http://identifiers.org/hco/3/GRCh38#172133374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27674901-C-A

172133379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674896-G-T

172133454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674841-A-G

172133454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674841-A-T

172133632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674662-T-C

172133740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674510-A-G

172133749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674501-T-C

172133767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674483-G-T

172134138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27674072-G-A

172134259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673971-G-A

172134299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673938-C-T

172134304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673933-T-C

172134376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673845-T-A

172134376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673845-T-C

172134376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673845-T-G

172134378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673843-T-C

172134378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673843-T-G

172134462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673760-T-G

172134636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673577-A-T

172134753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673471-T-C

172134904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673328-A-G

172135109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27673020-C-T

172135206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672932-C-G

172135290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672864-G-C

172135290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27672864-G-T

172137316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27671384-T-C

172137651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27671315-A-G

172137756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27671205-C-G

http://identifiers.org/hco/3/GRCh38#172138209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27670733-C-A

http://identifiers.org/hco/3/GRCh38#172138268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27670673-A-C

172138759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27670072-A-G

172138829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27670014-G-A

172138829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27670014-G-C

172138829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27670014-G-T

http://identifiers.org/hco/3/GRCh38#172138888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27669954-C-A

172138888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27669954-C-T

172138907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27669934-G-A

172138907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27669934-G-T

http://identifiers.org/hco/3/GRCh38#172138991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27669859-A-C

172139083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27669778-G-A

172139083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27669778-G-C

172139083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27669778-G-T

172139273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27669668-G-A

172139340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27669620-G-T

172139371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27669585-A-G

172140052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668797-C-T

http://identifiers.org/hco/3/GRCh38#172140125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27668732-A-C

172140216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668647-A-T

http://identifiers.org/hco/3/GRCh38#172140217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27668646-A-C

172140269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668572-C-G

172140374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668478-A-G

172140424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668434-T-C

172140428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668430-C-G

172140624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668261-G-A

172140637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668248-A-G

172140677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668209-T-C

172140726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668157-G-A

172140730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668153-T-G

172140787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668101-G-C

172140807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27668083-C-T

172140965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667945-G-T

172140979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667931-A-T

172141034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667907-A-G

172141268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667651-G-A

172141268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667651-G-T

172141339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667568-G-A

172141342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27667565-A-G

172142201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27666513-T-C

172142280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27666445-G-C

172142428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27666302-C-G

172147985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27665818-C-T

172148200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27665632-A-T

172148328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27665548-T-C

172148494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27665405-T-C

172148529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27665388-A-G

http://identifiers.org/hco/3/GRCh38#172148537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27665380-C-A

172148556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27665359-T-C

172148773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27665129-G-C

172150257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27663476-A-G

172150277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27663456-G-T

172150481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27663292-A-G

172150663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27663104-T-C

172150664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27663103-T-A

172150954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27662977-C-T

172150962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27662969-G-T

172151016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27662904-A-G

172153371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27661860-C-T

172153870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27661376-A-G

172153973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27661252-G-A

172154599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27660989-A-G

172154609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27660979-G-C

172154684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27660903-C-G

172154684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27660903-C-T

172155697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659294-A-G

172155946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27659083-A-G

172156127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27658926-C-G

172156283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27658761-A-G

172156532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27658506-A-G

172156960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27658108-A-G

172157029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27658047-T-C

http://identifiers.org/hco/3/GRCh38#172160181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27657155-A-C

172160312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27657049-C-T

172160457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27656940-C-T

172160655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27656755-T-C

172160664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27656746-C-G

172165373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27656160-T-C

172165399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27656135-G-C

172165656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27655805-A-G

172165834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27655650-A-G

172165914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27655571-A-G

172169151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 27653511-C-T

http://identifiers.org/hco/3/GRCh38#172169422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#27653276-A-C

172169435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 27653260-G-T

172169519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27653185-C-G

172169519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27653185-C-T

172169585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27653117-A-G

172171081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27650890-A-G

172171187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27650807-C-G

172171187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27650807-C-T

172171245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27650751-G-T

172171532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27650505-G-A

172171532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27650505-G-T

172171624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27650452-G-A

172171624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27650452-G-T

172171829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27650331-A-G

172171836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27650324-A-G

172171980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27650189-G-A

172172490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27649501-T-G

172172717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27649308-T-C

172172757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27649280-C-T

172172836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27649219-G-A

172172845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27649210-A-G

172172909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27649171-A-G

172173160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27648729-A-G

172173231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27648671-T-G

172173422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27648599-G-A

172174017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27648180-G-A

172174017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27648180-G-C

172174278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27647930-T-G

172174653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27647557-C-T

172174836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27647375-G-A

http://identifiers.org/hco/3/GRCh38#172174929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27647295-C-A

172174929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27647295-C-G

172174929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27647295-C-T

http://identifiers.org/hco/3/GRCh38#172174937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27647287-C-A

172174937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27647287-C-G

http://identifiers.org/hco/3/GRCh38#172174938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27647286-C-A

172174938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27647286-C-T

172175117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27647116-T-C

172175166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27647052-C-T

172175287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27646991-G-C

http://identifiers.org/hco/3/GRCh38#172175359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27646920-A-C

172175404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27646891-A-G

172175404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27646891-A-T

172175439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27646856-C-T

172175445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27646850-G-C

172175445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27646850-G-T

172175578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27646683-A-G

172179001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27646545-C-G

172180446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27645294-G-A

172180481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27645264-T-C

172180563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27645179-T-C

172180701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27645075-A-G

172180924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27644876-T-A

172180945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27644860-A-G

172181025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27644770-T-C

172182491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27643217-T-G

172182814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27642893-G-A

172183063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27642618-A-G

172183291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27642412-C-T

172183337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27642370-A-G

172184726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27641344-A-G

172185389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640258-A-G

172185389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640258-A-T

172185647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27640018-T-C

172185781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27639879-C-T

172186059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27639637-G-A

172186380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27639272-A-G

172186382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27639270-A-G

172186731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 27638955-C-T

172186783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638906-C-T

172186793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638896-A-G

172186857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638817-A-G

172186936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638762-T-C

172186996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638712-G-C

172187054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638655-T-C

172187059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638650-A-G

172187060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638649-G-A

172187060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638649-G-T

172187102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638608-T-C

172187102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638608-T-G

172187104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638606-G-C

172187104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638606-G-T

172187145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27638551-A-G

172187408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27638152-T-C

172187496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27638090-T-C

172187513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27638071-A-G

172187990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27637676-T-C

http://identifiers.org/hco/3/GRCh38#172187991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27637675-A-C

http://identifiers.org/hco/3/GRCh38#172187994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27637672-C-A

172187994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27637672-C-G

172189076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27637113-T-C

172189415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27636780-C-T

172194840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27634601-A-G

172194869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27634572-C-T

172194948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27634498-G-A

172195443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27634036-C-G

172195529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27633926-G-C

172198458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27632568-A-G

172198490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27632539-T-C

172198588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27632437-C-T

172198683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27632294-A-G

172198683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27632294-A-T

172198730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27632249-T-C

172200971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27631704-A-G

172201007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27631665-C-G

172201275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27631405-G-A

172201275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27631405-G-T

172201424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27630852-G-A

172201424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27630852-G-T

172201857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27630427-C-T

172201916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27630371-A-T

172201927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27630356-C-T

172202075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27630103-C-T

172202269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27629690-A-T

172202711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27629268-C-G

172202779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27629203-G-A

172202782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27629200-T-G

172202872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27629127-C-T

172202951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27629052-C-T

172203196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27628803-C-T

172203212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27628793-G-A

172203337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27628585-T-A

172203468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27628465-C-T

172203710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27628215-G-A

172203996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27627915-G-A

172203996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27627915-G-C

172203996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27627915-G-T

172204318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27627591-A-G

172204424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27627487-T-A

172204688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27627205-G-T

172204828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27627075-T-A

172204922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27626983-C-G

172205054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27626847-G-A

172205180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27626761-C-T

172205190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27626749-G-A

172205260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27626676-T-G

172205332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27626613-C-T

172205617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27626174-A-T

172205662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27626129-T-C

172205871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27625935-T-C

http://identifiers.org/hco/3/GRCh38#172205939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27625873-C-A

172206095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27625633-C-T

172206122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27625606-G-A

172211060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27622843-A-G

172211240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27622713-A-G

172211424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27622476-A-G

172211678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27622243-T-A

172211678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27622243-T-C

172212077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27621501-T-C

172212086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27621492-T-C

172213943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27620506-C-T

172214082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27620373-G-A

172214273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27620190-T-C

172214504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27619986-T-C

172214802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27619785-A-T

http://identifiers.org/hco/3/GRCh38#172214805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27619782-A-C

172214899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27619685-T-A

172215276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27619379-C-T

172215308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27619345-A-G

172215321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27619334-T-G

172215368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27619285-C-T

172215789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27618891-A-G

172216115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27618554-G-T

172216179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27618211-C-G

http://identifiers.org/hco/3/GRCh38#172216727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27617982-A-C

172216727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27617982-A-G

172216787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27617931-A-G

172217053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27617679-C-T

172217104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27617633-A-G

172217250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27617499-G-A

172217250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27617499-G-T

http://identifiers.org/hco/3/GRCh38#172217773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27617005-C-A

172217778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27617000-G-T

172217828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27616960-A-G

172217892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27616907-G-A

172217892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27616907-G-C

172217892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27616907-G-T

172218115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27616698-G-A

172218425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27616383-G-A

172218602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27616235-G-C

172218603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27616234-G-A

172218754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27616134-G-A

172218771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27616117-A-G

172218851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27616042-A-G

172218851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27616042-A-T

172218882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27616012-A-G

172222842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27614646-C-T

172223314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27613272-A-G

172223618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27612985-A-G

172223618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27612985-A-T

172223711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27612911-C-T

172223945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27612488-G-T

172223971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27612462-T-C

172224456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27611963-G-C

172224606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27611849-G-A

172226351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27610893-T-C

172226498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27610746-G-C

172226507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27610739-T-C

172226561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27610628-C-T

172226729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27610450-T-G

172226763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27610426-T-C

172226839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27610377-T-C

http://identifiers.org/hco/3/GRCh38#172226909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27610305-A-C

172226909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27610305-A-G

172226955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 27610259-A-G

172226983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27610232-A-G

http://identifiers.org/hco/3/GRCh38#172226998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27610217-C-A

172226998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27610217-C-T

172227015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27610200-A-G

172227047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27610168-G-T

http://identifiers.org/hco/3/GRCh38#172227083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27609816-C-A

172227083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27609816-C-T

http://identifiers.org/hco/3/GRCh38#172227093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27609806-C-A

172227093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27609806-C-T

172227111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27609788-A-G

http://identifiers.org/hco/3/GRCh38#172227153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27609750-C-A

172227155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27609748-T-C

172227205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27609720-G-A

http://identifiers.org/hco/3/GRCh38#172227229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27609696-C-A

172227243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27609682-T-C

172228233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27608782-A-G

http://identifiers.org/hco/3/GRCh38#172228407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27608607-A-C

http://identifiers.org/hco/3/GRCh38#172228452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27608565-C-A

172228452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27608565-C-G

172228452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27608565-C-T

172228683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27608332-T-C

172228871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27608052-A-G

172229026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27607902-T-C

172229484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27607140-C-T

172229628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27606989-A-G

172229640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27606977-G-A

172229868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27606487-G-A

172229868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27606487-G-C

172229995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27606361-A-G

172230093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27606265-T-C

172230639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27605949-G-T

172230873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27605762-A-G

172230929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27605713-A-G

172231304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27605369-A-G

172231305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27605368-G-T

172231365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27605290-G-T

172232958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27603455-A-G

172233089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27603354-T-G

172233548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27602921-G-A

172233625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27602670-C-T

172233851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27602465-T-C

172233904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27602425-G-A

172233948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27602386-G-A

172233950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27602384-A-G

172234095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27602275-C-G

172234167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27602222-A-G

172234374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27602052-C-T

172240777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27601019-T-C

172240893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600891-G-T

172240965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600613-A-G

172240985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600567-G-A

172241098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600419-G-T

172241110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600412-T-C

172241124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600399-A-T

172241311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600228-C-T

172243788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600101-T-C

http://identifiers.org/hco/3/GRCh38#172243935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27599966-C-A

172244506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27599456-G-A

172244548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27599415-G-A

http://identifiers.org/hco/3/GRCh38#172244573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27599394-C-A

http://identifiers.org/hco/3/GRCh38#172244600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27599364-C-A

172244600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27599364-C-T

172245059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27599252-A-T

172245996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27597597-C-T

172246128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27597461-C-T

172246360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27597160-C-T

172246416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27597108-A-G

172246493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27597040-A-G

172246505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27597024-C-T

http://identifiers.org/hco/3/GRCh38#172247090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27596669-C-A

172247110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27596647-T-G

172247309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27596449-A-G

172247331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27596419-G-T

172247388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27596400-G-A

172247388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27596400-G-T

172247396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27596392-G-A

172247419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27596373-G-T

172247464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27596363-T-C

172247502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27596352-C-T

172247602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27596252-A-G

172247638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27596216-C-G

172247683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27596171-A-G

172247683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27596171-A-T

172247807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27596047-G-A

http://identifiers.org/hco/3/GRCh38#172247970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27595947-C-A

172247970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595947-C-G

172247970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595947-C-T

172247973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595944-T-C

172248154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595810-A-G

172248407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595582-A-G

172248547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595456-T-C

172248802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595210-G-A

172248826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595186-C-T

172249387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27594423-G-C

172249650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27594151-A-G

172250245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593025-A-G

172250568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592717-G-A

172250568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592717-G-T

172250708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592583-A-G

http://identifiers.org/hco/3/GRCh38#172251173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27592447-C-A

172251271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27592375-T-C

172251406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27592240-A-G

172251563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592087-A-G

http://identifiers.org/hco/3/GRCh38#172251582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27592082-C-A

172251582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592082-C-G

172251640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592031-G-A

172251640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592031-G-T

172251671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592001-A-G

172252173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591524-G-A

172252173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591524-G-T

172252286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591385-G-A

http://identifiers.org/hco/3/GRCh38#172252543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27590635-A-C

172252729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590497-C-T

172252794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590439-A-G

172252922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590342-A-G

172253700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27588764-G-A

172253700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27588764-G-T

172254820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27587852-G-A

172254936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27587745-C-T

172254986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27587705-A-G

172255417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27587375-C-T

172255485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27587322-G-T

172256055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586940-C-G

172256361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586598-T-A

172256361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586598-T-G

172256434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586525-C-T

172258712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585207-C-T

172259063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584976-A-G

http://identifiers.org/hco/3/GRCh38#172259238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27584795-A-C

172259418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584638-G-A

172259516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584557-C-T

172259633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584459-T-C

172259767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584338-C-G

http://identifiers.org/hco/3/GRCh38#172259784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27584321-C-A

172259784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584321-C-T

172259804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584302-A-G

172259838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584270-G-A

172259924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584189-A-G

172260112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584010-G-T

http://identifiers.org/hco/3/GRCh38#172260342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27583798-C-A

172260433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27583716-A-T

172260534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27583614-G-T

172260814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27583425-T-C

http://identifiers.org/hco/3/GRCh38#172261319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27583019-C-A

http://identifiers.org/hco/3/GRCh38#172261367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27582968-A-C

172261631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27582753-G-A

http://identifiers.org/hco/3/GRCh38#172261768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27582672-A-C

172261823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27582615-G-T

172262293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27581513-T-C

172262715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27581202-C-G

172263005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580958-A-G

172263054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580915-C-T

172263090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580879-T-A

172263478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580557-T-A

172263489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580546-C-G

172263502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580533-G-T

172263632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580400-A-G

172263632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580400-A-T

172263757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580291-A-G

172266154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580113-A-G

172266413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27579924-A-G

172266556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27579850-T-G

172266716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27579706-C-T

172266802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27579614-A-T

172266999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27579386-C-T

172267065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27579342-G-C

172267702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27578906-A-G

172268039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27578600-C-T

172268129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27578518-A-G

172268202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27578450-C-T

172268604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27578067-T-C

172270015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27577391-C-T

172270163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27577131-T-G

172270253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27577008-C-T

172270258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27577006-G-A

172270461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576852-A-G

172270575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576755-G-A

172270744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576605-T-C

172270751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576598-C-G

172270774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576575-A-G

172270981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576355-T-C

172271072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576268-C-G

172271165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576227-A-G

172271166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576226-T-C

172271191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576198-A-G

172271370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576057-T-C

172271381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576046-T-A

172271501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575924-C-T

172271748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575723-T-A

172272056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575437-A-G

172272482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575081-C-T

172272622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574971-T-G

172273271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574351-A-G

http://identifiers.org/hco/3/GRCh38#172273311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27574316-A-C

http://identifiers.org/hco/3/GRCh38#172273339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27574292-A-C

172273403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574244-C-G

172273403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574244-C-T

172273419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574230-G-C

172273911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573739-G-A

172273930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573720-T-C

172274002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573657-C-T

172274191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573465-T-C

172275307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569546-G-T

172275346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569511-T-C

172275384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569472-A-G

172275556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569307-T-G

172275644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569255-G-A

172275753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569166-G-A

172275757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569162-A-G

172275795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569141-C-T

172275916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569022-G-T

172278115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565741-A-G

172278150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565707-T-A

172278173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565684-C-T

172278188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565668-A-G

172278188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565668-A-T

172278312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565548-C-G

172278470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565406-G-A

172278603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565276-T-A

172278756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565150-G-A

172279088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565016-C-T

172279227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564894-C-G

172279227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564894-C-T

172279271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564868-C-T

172279345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564791-C-T

172284374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563967-G-A

172284670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563739-G-A

http://identifiers.org/hco/3/GRCh38#172284784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27563662-C-A

172284798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563649-T-C

172284838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563623-G-A

172285014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563488-A-G

172285234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563309-C-G

172285408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563144-T-A

http://identifiers.org/hco/3/GRCh38#172285433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27563119-C-A

172285458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563097-A-G

172286066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562553-T-A

172286066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562553-T-C

172286066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562553-T-G

172286079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562543-G-A

172286079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562543-G-C

172286079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562543-G-T

172286118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562531-T-C

172286122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562527-G-A

172286122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562527-G-T

172286223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562437-C-T

172286307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562370-A-G

172286856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27561856-T-C

172287158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27560891-G-A

172287180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27560869-G-T

172287348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27560688-G-A

172287373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27560664-C-T

172289622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27560092-T-C

172289719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559987-G-A

172289835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559880-C-G

172289904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559798-C-T

172289916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559786-G-T

172289975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559729-T-G

172290052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559642-T-G

172290262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559435-A-G

http://identifiers.org/hco/3/GRCh38#172290570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27559158-C-A

172290709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559023-A-G

172290811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558937-T-G

172290895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558860-T-C

172291217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558684-C-G

172291263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558649-T-C

172291636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558474-G-A

172291705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558410-C-T

172291710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558405-G-A

172291780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558350-C-T

172291825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558309-G-A

172291826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558308-C-T

172291854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558280-T-G

172291887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558242-A-G

172292146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558038-G-C

172292151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558033-A-G

172292423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27557822-G-C

172292568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27557686-G-A

172292568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27557686-G-T

172292569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27557685-T-C

172293094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27557229-G-T

172293148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27557195-C-T

172293316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27557058-G-A

172293316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27557058-G-T

172293462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556872-G-A

172293573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556755-A-G

172293901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556440-G-A

172293935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556396-T-G

172293942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556389-A-G

172293942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556389-A-T

172294097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556229-A-T

172294099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556227-A-G

172294140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556184-T-G

172294167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556171-T-C

172295411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27555644-G-C

172295528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27555527-C-T

172295552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27555502-C-T

172295604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27555410-G-A

172295604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27555410-G-C

172295611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27555403-A-G

172295636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27555374-A-G

172295745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27555265-A-G

http://identifiers.org/hco/3/GRCh38#172296213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27554985-C-A

172296304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554916-C-T

http://identifiers.org/hco/3/GRCh38#172296477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27554740-C-A

172296502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554729-G-T

172296609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554625-C-T

172297963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553738-T-C

172297974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553727-G-A

172298063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553585-A-G

http://identifiers.org/hco/3/GRCh38#172298118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27553521-A-C

172298193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553437-C-T

172298301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553367-G-T

172298353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553313-C-G

172298583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553122-A-G

172298639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27553065-T-A

http://identifiers.org/hco/3/GRCh38#172298690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27553018-A-C

172298690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553018-A-G

172298809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552897-A-G

172298809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552897-A-T

172298815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552891-T-C

172298849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552881-G-A

172298849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552881-G-T

172298857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552874-T-C

172298860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552871-T-C

172298886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552845-T-C

172298886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552845-T-G

http://identifiers.org/hco/3/GRCh38#172298904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27552822-C-A

172298904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552822-C-T

172298917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552809-G-A

172298917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552809-G-C

172298917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552809-G-T

http://identifiers.org/hco/3/GRCh38#172298939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27552789-C-A

172298939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552789-C-G

172298939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552789-C-T

172299145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552237-T-A

172299155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552227-G-A

172299158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552224-C-T

172299180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552202-C-G

http://identifiers.org/hco/3/GRCh38#172299480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27551949-C-A

172299498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551934-G-T

172299548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551915-A-T

http://identifiers.org/hco/3/GRCh38#172299761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27551757-A-C

172300113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551158-C-G

172300113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551158-C-T

172300135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551136-C-T

172300180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551106-T-A

172300277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551019-T-C

172300375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27550927-C-G

172300384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27550919-G-C

172300483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27550838-A-T

http://identifiers.org/hco/3/GRCh38#172300489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27550832-A-C

172302685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27549420-T-A

172302685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27549420-T-C

172302693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27549412-C-T

172303319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548464-G-A

172303322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548461-A-G

172303323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548460-A-G

172303528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548256-G-A

172303700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548097-T-C

http://identifiers.org/hco/3/GRCh38#172303717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27548080-C-A

172303814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27547877-G-C

172305874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27546196-C-T

172306015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27546053-A-G

172306783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27545894-C-T

172306865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27545801-G-A

172306909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27545758-T-C

172306962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27545699-A-T

http://identifiers.org/hco/3/GRCh38#172307002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27545646-C-A

172307002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27545646-C-G

172307002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27545646-C-T

172307012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27545636-G-C

172307012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27545636-G-T

http://identifiers.org/hco/3/GRCh38#172307161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27545495-A-C

172307161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27545495-A-G

172307162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27545494-G-A

http://identifiers.org/hco/3/GRCh38#172307242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27545431-A-C

172307242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27545431-A-G

172307242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27545431-A-T

172307315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27545362-T-C

172307370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27545303-G-A

http://identifiers.org/hco/3/GRCh38#172307517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27545156-C-A

172307649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27545139-A-G

172307757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27545096-G-A

http://identifiers.org/hco/3/GRCh38#172307870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27544986-C-A

172307946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544921-A-G

172308060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544824-T-C

172308064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544820-A-G

172308581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544432-G-T

172308611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544415-C-G

172308625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544401-C-T

http://identifiers.org/hco/3/GRCh38#172308640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27544386-A-C

172308789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544239-C-T

172308860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544176-T-C

172308877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544157-G-A

172308920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544116-A-G

172308988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544049-T-C

172309098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543987-G-T

172309167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543916-T-A

172309716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543475-C-G

172309736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543455-A-G

172309798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543393-C-T

172309860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543346-A-G

172309867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543339-T-G

172309885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543321-G-T

172309886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543319-A-G

172309985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543223-C-G

172310279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542970-A-T

172310337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542913-T-G

172310619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542598-T-A

172310708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542529-T-A

172310708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542529-T-C

172310894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27542371-T-A

http://identifiers.org/hco/3/GRCh38#172310952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27542329-C-A

172311076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542250-A-G

172311076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542250-A-T

172311190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542144-T-C

172311242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542092-C-T

172311254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542083-A-G

172311264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542073-T-A

http://identifiers.org/hco/3/GRCh38#172311345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27541991-C-A

172311345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27541991-C-T

172312181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27541700-G-A

172312288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27541602-C-T

172312308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27541582-G-C

172313194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27539836-C-T

172313319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27539758-G-T

172313375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27539704-A-G

172313494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27539594-G-A

172313494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27539594-G-T

172313524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27539553-C-T

http://identifiers.org/hco/3/GRCh38#172313556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27539520-A-C

172314333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27538809-G-A

172314333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27538809-G-T

172314355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27538787-G-C

172314413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27538326-A-G

172314837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27538019-G-A

172314860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27538010-C-T

172314880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27537990-C-G

172314930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27537949-A-G

172314983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27537895-T-C

http://identifiers.org/hco/3/GRCh38#172315025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27537858-A-C

172315604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27537619-C-T

172315612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27537611-G-A

172316427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27537048-A-T

172316438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27537037-T-C

172316526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27536933-G-A

172318011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27536069-C-T

172318173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27536025-G-A

172318173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27536025-G-T

172318260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27535941-C-T

http://identifiers.org/hco/3/GRCh38#172318340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27535850-A-C

172318514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27535780-G-A

172318514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27535780-G-T

172318522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27535772-C-T

172318783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27535202-G-A

172319459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533956-A-G

172319567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533847-T-G

172319698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533748-T-G

172319819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533641-C-G

http://identifiers.org/hco/3/GRCh38#172320054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27533404-A-C

172320098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533354-G-A

172320237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533260-G-A

172320241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533256-A-G

172320241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533256-A-T

172320247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533251-G-A

172320295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533196-G-C

172320679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27532898-G-A

172320804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27532773-T-C

172321066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27532504-T-C

172321097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27532474-G-C

172321862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27531661-G-A

172321862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27531661-G-C

172321862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27531661-G-T

172322054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27531616-A-G

172322095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27531586-T-C

172322226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27531467-G-A

172322393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27531336-C-T

172322466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27531272-C-T

172322472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27531266-C-T

172322630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27531159-A-T

172322635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27531154-C-G

172322635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27531154-C-T

172322756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27530994-C-G

172322821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27530914-G-A

172322996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27530771-T-C

172323058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27530689-T-C

172323758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27527924-G-A

172323952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27528018-A-G

172324000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27528062-T-C

172324706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27528626-A-G

172324978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27528886-G-A

172325256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27529731-C-G

172325539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27529985-A-T

172325633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27530111-T-G

http://identifiers.org/hco/3/GRCh38#172325807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27530274-C-A

172326757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27526961-A-G

http://identifiers.org/hco/3/GRCh38#172326806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27526912-C-A

172326871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27526848-A-G

172327057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27526667-A-G

172327058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27526666-T-C

172327061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27526663-G-C

172327063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27526661-T-C

172327068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27526656-G-T

172327141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27526571-A-G

172327268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27526462-T-A

172328446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27525131-A-T

172328561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27525028-G-A

172328650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524949-A-G

http://identifiers.org/hco/3/GRCh38#172328671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27524916-C-A

http://identifiers.org/hco/3/GRCh38#172328725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27524854-C-A

172328850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524731-A-T

http://identifiers.org/hco/3/GRCh38#172328877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27524713-C-A

172328877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524713-C-T

172328882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524708-T-G

172328901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524689-T-A

172328901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524689-T-C

172328901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524689-T-G

172328918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524662-T-A

172328918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524662-T-G

172328931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524530-T-A

172328935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524526-T-C

172329030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27524415-A-G

http://identifiers.org/hco/3/GRCh38#172329101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27524344-C-A

172329101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524344-C-T

172329135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524311-T-C

172329165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524285-T-C

172329165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524285-T-G

172329177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524273-A-G

172329177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524273-A-T

172329191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524269-A-G

172329248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524218-A-G

http://identifiers.org/hco/3/GRCh38#172329266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27524200-C-A

172329266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524200-C-T

172329332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524084-T-A

172329336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524080-G-T

http://identifiers.org/hco/3/GRCh38#172329337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27524079-A-C

172329337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524079-A-G

172329356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524058-T-C

http://identifiers.org/hco/3/GRCh38#172329366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27524048-A-C

172329366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27524048-A-T

172329393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523958-T-C

http://identifiers.org/hco/3/GRCh38#172329406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27523945-C-A

172329406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523945-C-T

172329470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523863-G-A

172329470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523863-G-T

http://identifiers.org/hco/3/GRCh38#172329471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27523862-C-A

http://identifiers.org/hco/3/GRCh38#172329480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27523857-C-A

172329509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523838-G-T

172329519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523828-A-G

172329594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523752-T-C

172329651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523700-A-G

172329748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523626-C-G

172329997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523380-T-C

172330046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523345-G-A

172330486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523222-A-G

http://identifiers.org/hco/3/GRCh38#172330506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27523211-C-A

172330506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523211-C-T

172330507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27523210-T-A

172330557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27523171-G-A

172330557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27523171-G-T

172330560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27523168-G-A

172330593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27523135-C-T

172330594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27523134-C-T

172330621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27523107-G-A

http://identifiers.org/hco/3/GRCh38#172330784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27522979-C-A

http://identifiers.org/hco/3/GRCh38#172330804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27522961-A-C

172330804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27522961-A-G

172330812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27522953-A-G

http://identifiers.org/hco/3/GRCh38#172332274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27522434-C-A

172332367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27522324-A-G

http://identifiers.org/hco/3/GRCh38#172332405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27522297-A-C

172332469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27522227-A-G

172332580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27522101-T-C

http://identifiers.org/hco/3/GRCh38#172332672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#27522005-C-A

172332856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27521829-A-G

172332960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27521746-G-A

172332960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27521746-G-T

172332962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27521744-T-C

172333057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27521654-A-G

172333057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27521654-A-T

http://identifiers.org/hco/3/GRCh38#172333246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27521468-C-A

172333246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27521468-C-T

172333287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27521423-T-C

172333381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27521324-G-A

172333390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27521315-C-T

172333394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27521311-T-C

172334771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27520158-A-G

172334870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27520058-T-C

172335028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27519903-A-G

http://identifiers.org/hco/3/GRCh38#172335211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27519771-C-A

172335211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27519771-C-T

172335297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27519719-A-T

172335567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27519458-T-G

172335764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27519249-G-A

172335784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27519227-A-G

172335814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27519192-A-G

172335860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27519155-G-A

172336088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27518985-A-G

172336214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27518876-T-G

172336416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27518690-C-T

172337241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27518074-A-G

http://identifiers.org/hco/3/GRCh38#172337538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27517786-C-A

172341080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27515972-G-A

172341199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense variant
orthologous variants: 27515855-G-T

172341300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27515754-A-G

172341300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27515754-A-T

172341330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27515727-G-A

172341519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27515558-T-A

172341546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27515531-G-A

172341611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27515468-T-C

172341648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27515454-A-T

172342294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27514881-A-G

172342474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27514712-C-G

172342724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27514470-G-A

172342724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27514470-G-T

172342830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27514362-C-T

172342835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27514357-A-G

172342948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27514258-A-G

172343035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, missense_variant
orthologous variants: 27514173-A-G

172343061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, missense_variant
orthologous variants: 27514147-T-G

172343188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27514024-T-C

172343219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27513989-T-C

172343627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27513676-A-G

172343668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27513636-A-G

172343674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27513632-T-C

http://identifiers.org/hco/3/GRCh38#172344048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27513073-C-A

172344052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27513069-G-A

172344163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 27512959-G-C

http://identifiers.org/hco/3/GRCh38#172344178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27512944-C-A

172344178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 27512944-C-T

172344395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27512774-T-A

172344501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27512672-G-C

172344517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27512656-C-G

172344521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27512652-G-A

http://identifiers.org/hco/3/GRCh38#172344553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27512619-C-A

172344553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27512619-C-T

172344762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27512115-T-A

172344789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27512092-A-G

172345907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511599-G-T

172346108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511453-A-G

172346146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511411-G-A

172346146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511411-G-C

172346146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511411-G-T

http://identifiers.org/hco/3/GRCh38#172346151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27511406-A-C

http://identifiers.org/hco/3/GRCh38#172346164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27511393-A-C

172346164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511393-A-G

172346204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511354-T-C

172346204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511354-T-G

172346222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511336-A-T

172346254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511308-T-G

http://identifiers.org/hco/3/GRCh38#172346266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27511296-C-A

172346266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511296-C-T

http://identifiers.org/hco/3/GRCh38#172346300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27511273-C-A

172346300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511273-C-T

172346307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511266-G-A

172346307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27511266-G-T

172346327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 27511247-T-C

http://identifiers.org/hco/3/GRCh38#172346525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27511047-C-A

http://identifiers.org/hco/3/GRCh38#172346533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27511039-C-A

172346533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27511039-C-G

http://identifiers.org/hco/3/GRCh38#172347171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27510783-C-A

172347172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27510782-T-G

http://identifiers.org/hco/3/GRCh38#172347173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27510781-C-A

172347317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27510640-A-G

http://identifiers.org/hco/3/GRCh38#172347433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27510528-C-A

172347684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27509973-G-A

172347728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27509947-A-T

172347822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27509853-C-T

172347845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27509752-G-C

172348030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27509563-T-C

172348236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27509375-A-G

172348259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27509364-G-A

172349595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27508300-G-A

172349798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27508102-G-A

172349871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27508080-G-T

172350021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27507961-A-G

172350087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27507890-T-C

172350087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27507890-T-G

172350089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27507888-G-A

172350234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27507756-T-C

172350234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27507756-T-G

172350965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27507056-C-T

http://identifiers.org/hco/3/GRCh38#172350997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27507025-A-C

172351149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27506914-T-G

172351239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27506852-G-C

172351351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27506771-G-A

172352765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27505778-G-T

172354839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27503291-A-T

172354845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27503261-G-T

172354903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27503206-A-G

172354903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27503206-A-T

172354904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27503205-T-C

172355016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27503124-C-G

172355320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27502855-T-G

172355438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27502734-C-T

172355674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27501219-A-G

172355695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27501193-C-T

172355737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27501169-G-T

172355858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, undefined
orthologous variants: 27501072-T-C

http://identifiers.org/hco/3/GRCh38#172355861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#27501069-C-A

172355909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27501043-C-T

172356044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27500927-T-A

172356161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, undefined
orthologous variants: 27500812-G-C

172356172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron_variant, undefined
orthologous variants: 27500801-G-A

172356592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27500487-T-C

172356853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27500254-C-T

172356874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27500239-T-G

172356908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27500208-C-G

172356913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27500201-C-T

172357024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27500091-A-G

172357084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27500039-T-C

172358080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27499106-C-G

172358100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27499085-C-T

172358138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27499047-G-C

172358145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27499040-A-G

http://identifiers.org/hco/3/GRCh38#172359141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27498298-C-A

172359171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27498267-A-G

172359211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27498258-T-A

172359454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27498000-T-C

172359703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27497770-A-G

172359872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27497635-C-G

172359877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27497630-T-A

172359966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27497554-T-G

172359987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27497546-A-G

172360329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27497181-T-C

http://identifiers.org/hco/3/GRCh38#172360367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27497143-A-C

172360398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27497112-G-A

172360930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27496565-C-T

172362563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27494382-G-A

172362569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27494376-T-G

172362662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense variant
orthologous variants: 27494288-G-C

172362850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27494100-G-T

172362942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27494029-T-A

http://identifiers.org/hco/3/GRCh38#172362978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27493982-C-A

172362978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27493982-C-T

172363070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27493901-T-C

172363388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27493579-A-G

172363563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27493407-A-G

172364116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27491680-T-C

172364127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27491674-C-T

172364251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27491553-T-C

172364427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27491388-T-G

172364552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27491324-C-T

172364654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27491236-A-T

http://identifiers.org/hco/3/GRCh38#172364717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27491172-A-C

172364775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27491099-G-A

172364946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27490923-T-G

172365013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27490855-C-G

172367031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27490048-G-A

http://identifiers.org/hco/3/GRCh38#172367222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27489881-A-C

http://identifiers.org/hco/3/GRCh38#172367246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27489856-A-C

172367246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27489856-A-G

172367282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27489820-T-G

172367472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27489630-A-G

172367502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27489600-C-T

172367665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27489436-G-A

http://identifiers.org/hco/3/GRCh38#172368334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27488942-C-A

http://identifiers.org/hco/3/GRCh38#172368358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27488918-C-A

172368386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27488891-C-T

http://identifiers.org/hco/3/GRCh38#172368439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27488851-A-C

http://identifiers.org/hco/3/GRCh38#172368441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27488849-C-A

172368441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27488849-C-T

172369759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27487663-G-T

172369839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27487575-C-G

172369856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27487562-A-G

http://identifiers.org/hco/3/GRCh38#172369857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27487561-C-A

172369943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27487445-G-A

172369943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27487445-G-T

http://identifiers.org/hco/3/GRCh38#172369948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27487440-C-A

172369950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27487438-A-G

172370161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27487219-C-G

172370320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27487056-A-G

http://identifiers.org/hco/3/GRCh38#172370403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27486972-A-C

172370603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27486767-T-C

172370654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27486716-A-T

172374177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27486084-G-A

172375208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27485424-A-G

172375500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27485127-G-T

172375708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27484944-G-A

172375708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27484944-G-C

172376212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27484456-T-A

172376792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27483898-G-C

172376910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27483851-A-G

172376926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27483833-A-G

172376926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27483833-A-T

172377297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27483532-T-C

172377489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27483456-G-A

172377534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27483413-T-C

http://identifiers.org/hco/3/GRCh38#172377541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27483406-C-A

172377546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27483401-C-T

172378167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27483281-G-A

172378167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27483281-G-T

http://identifiers.org/hco/3/GRCh38#172378461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27482987-C-A

172378461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482987-C-T

172378476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482972-G-A

172378476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482972-G-C

http://identifiers.org/hco/3/GRCh38#172378547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27482889-C-A

172378547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482889-C-T

172378641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482814-G-C

172378683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482754-G-A

172378683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482754-G-C

172378866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482544-C-T

http://identifiers.org/hco/3/GRCh38#172379049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27482410-C-A

172379073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482396-G-A

172379086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482391-C-T

172379126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482355-G-A

172379163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482312-T-A

172379163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482312-T-C

172379289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482222-G-A

172379311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482200-A-G

172379384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482123-C-G

172379391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482108-C-T

172379432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27482066-C-G

172379493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27481996-G-A

172379522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27481967-A-G

172379561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27481932-G-C

172379567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27481926-T-C

172379641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27481893-T-C

172379651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27481884-C-G

172379656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27481879-G-A

172379670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27481865-T-C

172379670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27481865-T-G

172379919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27481621-G-T

172380095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27481469-A-G

172380183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27481379-A-G

http://identifiers.org/hco/3/GRCh38#172380341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27481143-A-C

172380436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27481039-A-G

172380725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27480532-G-T

172380742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27480515-G-A

172380865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27480400-A-T

http://identifiers.org/hco/3/GRCh38#172380870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27480395-C-A

http://identifiers.org/hco/3/GRCh38#172380912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27480354-C-A

172380912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27480354-C-T

172380977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense variant
orthologous variants: 27480297-A-G

172381138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27480153-G-A

172381138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27480153-G-T

172381149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27480141-C-T

172381381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27479916-T-C

172381388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27479911-C-T

172381402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27479897-A-G

172383406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27479880-G-A

172383430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27479856-T-C

172383529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27479748-G-C

172383529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27479748-G-T

172383964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27479398-G-T

172384002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27479360-A-G

http://identifiers.org/hco/3/GRCh38#172384393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27478957-C-A

172384469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27478889-A-G

172384561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27478817-T-G

http://identifiers.org/hco/3/GRCh38#172384601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27478779-C-A

172384601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27478779-C-T

172385017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27478429-A-G

172385227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27478215-C-T

172385289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27478153-A-G

172385292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27478150-A-G

http://identifiers.org/hco/3/GRCh38#172385308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27478127-C-A

172385308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27478127-C-G

172385995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27477936-G-A

http://identifiers.org/hco/3/GRCh38#172386904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27477431-A-C

http://identifiers.org/hco/3/GRCh38#172386939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27477396-C-A

172387600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27477216-A-G

http://identifiers.org/hco/3/GRCh38#172387733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27477107-C-A

172387809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27477043-A-G

172387845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27477002-G-A

172387911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27476929-A-G

172387981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27476873-C-T

172388091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27476798-T-A

172388722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27476221-A-T

172388744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: intron variant
orthologous variants: 27476195-G-A

172397230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: missense variant
orthologous variants: 27473683-C-T

http://identifiers.org/hco/3/GRCh38#172397554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27473362-C-A

172397742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27473154-T-A

172397868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27473038-T-C

172397868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27473038-T-G

172398137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27472786-G-T

172398400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27472563-G-T

http://identifiers.org/hco/3/GRCh38#172398545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27472411-C-A

172398974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27472009-G-A

172399244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27471738-A-G

172399244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27471738-A-T

172399416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27471564-G-A

172399513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27471470-A-G

172399619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27471364-T-A

172399671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27471313-G-A

172399752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27471252-A-G

http://identifiers.org/hco/3/GRCh38#172399757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27471247-C-A

172399772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27471235-G-A

172399902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27471105-T-A

http://identifiers.org/hco/3/GRCh38#172399905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27471102-A-C

172399905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27471102-A-G

172400219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: 27470793-A-G

http://identifiers.org/hco/3/GRCh38#172400323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#27470689-C-A