34956631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron variant
orthologous variants: 42915807-A-G

34956883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron variant
orthologous variants: 42915992-T-C

34957038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron variant
orthologous variants: 42916132-A-G

34957128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron variant
orthologous variants: 42916304-C-G

34957128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron variant
orthologous variants: 42916304-C-T

34957162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron variant
orthologous variants: 42916351-C-T

34957207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron variant
orthologous variants: 42916383-T-C

34957528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42916657-T-C

34957584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42916718-C-T

34957692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42916823-G-A

34957701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42916833-A-G

http://identifiers.org/hco/9/GRCh38#34957833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42916936-A-C

http://identifiers.org/hco/9/GRCh38#34957834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42916937-C-A

34957834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916937-C-G

34957834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916937-C-T

34957839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42916942-C-T

34957840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42916943-C-T

34957889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42916988-C-T

34957908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42917006-C-G

34957981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42917078-G-A

http://identifiers.org/hco/9/GRCh38#34958230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42917260-C-A

34958230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42917260-C-T

http://identifiers.org/hco/9/GRCh38#34958272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42917287-C-A

34958272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42917287-C-T

34958308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42917323-G-A

34958462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42917475-C-G

34958462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42917475-C-T

34958526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42917521-T-A

34958526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42917521-T-C

34958792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42917754-G-A

34958792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42917754-G-C

34959086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42918018-C-T

34959105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42918037-C-T

34959141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42918071-G-A

http://identifiers.org/hco/9/GRCh38#34959360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42918251-C-A

34959567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42918443-G-A

http://identifiers.org/hco/9/GRCh38#34959612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42918484-A-C

34960071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42918852-T-C

34960137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42918915-G-A

34960201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42918977-T-A

34960201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42918977-T-C

34960655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42920210-T-C

34960680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42920235-C-G

34961608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921070-C-T

34961639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921100-G-A

34962080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921510-G-A

34962247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921677-C-T

34962506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42921930-T-G

34963036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42922513-G-A

34963095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42922563-C-G

34963200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42922657-A-G

http://identifiers.org/hco/9/GRCh38#34963233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42922683-A-C

34963245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42922702-A-T

34963252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42922709-T-C

34963520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42923150-C-G

34963520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42923150-C-T

34964597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42924440-T-G

34964795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42924634-A-G

34964830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42924657-G-A

34964915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42924742-T-A

34964984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42924812-C-T

34965320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42925148-A-T

34965741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42925579-G-A

34965859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42925696-T-A

34965859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42925696-T-C

34966050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42925864-G-A

34966050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42925864-G-T

34966068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42925882-A-G

34966080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42925895-C-G

34966166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42925970-A-G

34966189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42925996-T-C

34969114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42931405-A-G

34969172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42931459-G-A

34969219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42931507-G-A

34969219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42931507-G-C

34969226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42931514-C-T

34969264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42931550-C-G

34970097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42932374-G-A

34970110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42932387-T-A

http://identifiers.org/hco/9/GRCh38#34970243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42932513-C-A

34970344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42932607-C-G

34970362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42932625-C-G

34970506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42932742-G-A

34970649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42932897-G-A

34970649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42932897-G-C

34970805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42933029-T-G

34970840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42933063-C-T

34971122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42933478-G-A

http://identifiers.org/hco/9/GRCh38#34971176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42933533-C-A

http://identifiers.org/hco/9/GRCh38#34971214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42933574-C-A

34971571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42933892-G-A

http://identifiers.org/hco/9/GRCh38#34971616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42933937-C-A

34971616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42933937-C-T

34971686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934007-C-T

34971688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934009-G-C

34971688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934009-G-T

34971697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934018-G-A

34971708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934029-T-C

34971723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934052-G-A

34971723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934052-G-C

34971723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934052-G-T

34971733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934067-G-A

34971733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934067-G-C

34971748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934082-G-A

http://identifiers.org/hco/9/GRCh38#34971789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42934122-A-C

http://identifiers.org/hco/9/GRCh38#34971794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42934127-A-C

34971943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934333-A-G

34972198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934533-A-G

34972199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934534-A-G

34972236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934561-G-A

34972236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934561-G-C

34972237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934562-G-T

34972241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934566-A-T

34972245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934570-G-A

34972245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934570-G-T

34972357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42934644-T-G

34972370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42934657-G-A

34972417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42934704-C-T

http://identifiers.org/hco/9/GRCh38#34972501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42934788-C-A

34972586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42934871-G-C

34973289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42935207-A-G

34973416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42935331-C-T

34973459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42935374-G-A

34973505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42935420-C-T

34973801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42935713-G-A

34973867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42935780-A-G

http://identifiers.org/hco/9/GRCh38#34974387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42936062-A-C

34974387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42936062-A-G

34974452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42936125-A-G

34974495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42936167-C-G

34974495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42936167-C-T

34975181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937007-G-C

34975711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937401-A-T

34975880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937559-C-T

34976024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937707-T-A

34976038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937721-G-T

http://identifiers.org/hco/9/GRCh38#34976076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42937756-C-A

34976076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937756-C-T

http://identifiers.org/hco/9/GRCh38#34976082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42937762-C-A

http://identifiers.org/hco/9/GRCh38#34976133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42937823-A-C

34976133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937823-A-G

34976134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937824-G-C

34976243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42937931-G-A

http://identifiers.org/hco/9/GRCh38#34976303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42937988-C-A

http://identifiers.org/hco/9/GRCh38#34976434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42938076-A-C

34976716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42938354-G-A

http://identifiers.org/hco/9/GRCh38#34976723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42938361-C-A

34976746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938384-G-A

34976755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938391-G-A

34976826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938455-G-A

34976826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938455-G-T

34976867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938496-T-C

34976875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938504-A-G

34976875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938504-A-T

34976878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938507-G-A

34976878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938507-G-T

34976905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938534-G-A

34977032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938579-G-T

http://identifiers.org/hco/9/GRCh38#34977034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42938581-C-A

34977034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938581-C-G

34977034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938581-C-T

34977106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42938638-A-G

http://identifiers.org/hco/9/GRCh38#34977251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42938783-C-A

34977251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42938783-C-T

34977261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938793-C-G

34977261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938793-C-T

http://identifiers.org/hco/9/GRCh38#34977277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42938821-C-A

34977314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938856-A-T

34977358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938900-T-C

34977359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938901-G-A

34977359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938901-G-T

34977369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938911-T-A

34977369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938911-T-C

http://identifiers.org/hco/9/GRCh38#34977432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42938972-C-A

34977432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42938972-C-T

http://identifiers.org/hco/9/GRCh38#34977439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42938979-C-A

34977494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939033-G-A

34977495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939035-G-A

34977495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939035-G-T

34977496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939036-G-A

34977496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939036-G-T

34977498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939038-A-T

34977510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939050-A-G

34977595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42939135-A-G

34977596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42939136-G-A

34977596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42939136-G-C

http://identifiers.org/hco/9/GRCh38#34977615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42939155-C-A

34977615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42939155-C-G

34977615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42939155-C-T

http://identifiers.org/hco/9/GRCh38#34977653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42939193-C-A

http://identifiers.org/hco/9/GRCh38#34977725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42939265-C-A

34977725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939265-C-T

34977791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939328-A-G

34977791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939328-A-T

34977853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939391-G-T

34977891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939429-G-T

34977912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939450-C-T

34977955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939463-G-A

34977955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42939463-G-T

http://identifiers.org/hco/9/GRCh38#34978185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42939680-C-A

34978279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42939774-A-G

34978295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42939784-T-C

http://identifiers.org/hco/9/GRCh38#34978301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42939790-C-A

34978301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42939790-C-T

34978315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42939804-G-A

34978315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42939804-G-T

http://identifiers.org/hco/9/GRCh38#34978506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42940017-C-A

34978542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940049-G-T

http://identifiers.org/hco/9/GRCh38#34979135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42940599-C-A

34979135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940599-C-T

http://identifiers.org/hco/9/GRCh38#34979148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42940611-A-C

34979148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940611-A-G

http://identifiers.org/hco/9/GRCh38#34979160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42940624-C-A

34979160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940624-C-T

34979166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940630-G-T

34979270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940728-G-A

34979270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940728-G-T

34979362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940787-G-A

34979394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940823-G-A

34979394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940823-G-T

34979482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940906-G-A

34979482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940906-G-T

34979523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940946-G-A

34979523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42940946-G-T

34979585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941005-T-C

34979675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941099-G-A

34979675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941099-G-T

34979703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941127-G-A

34979703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941127-G-T

34979727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941150-G-A

34979727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941150-G-C

34979727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941150-G-T

34979737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941160-G-T

34979751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941174-G-A

34979772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941195-G-A

34979772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941195-G-T

http://identifiers.org/hco/9/GRCh38#34979811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42941234-A-C

34979910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941497-A-G

http://identifiers.org/hco/9/GRCh38#34980054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42941645-C-A

http://identifiers.org/hco/9/GRCh38#34980198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42941778-C-A

34980198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42941778-C-T

34980251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 42941832-G-A

34980260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42941841-A-T

34980275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42941856-C-G

34980275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42941856-C-T

34980282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42941863-A-G

http://identifiers.org/hco/9/GRCh38#34980501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42941958-C-A

34980518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42941971-A-G

34980592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942043-G-A

34980592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942043-G-C

34980592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942043-G-T

http://identifiers.org/hco/9/GRCh38#34980610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42942061-C-A

34980610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942061-C-T

34980611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942062-A-G

34980752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942181-G-A

34980917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942372-G-A

34980917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942372-G-T

34980968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942420-C-T

34981063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942499-G-A

34981063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942499-G-T

http://identifiers.org/hco/9/GRCh38#34981078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42942513-C-A

34981294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942723-G-A

34981379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942807-G-T

http://identifiers.org/hco/9/GRCh38#34981464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42942880-A-C

34981511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942926-G-A

34981511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942926-G-T

http://identifiers.org/hco/9/GRCh38#34981533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42942948-C-A

34981533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942948-C-T

34981547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942966-A-G

34981568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42942989-G-T

34981671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42943386-C-T

34981789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42943455-C-G

http://identifiers.org/hco/9/GRCh38#34981820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42943487-C-A

34982033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42943694-G-A

34982033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42943694-G-T

34982081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42943743-G-T

34982246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42943866-C-T

34982265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42943884-G-T

34982357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42943969-C-T

34982391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42944003-G-A

34982391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42944003-G-C

34982391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42944003-G-T

http://identifiers.org/hco/9/GRCh38#34982476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#42944084-C-A

34982476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42944084-C-T

34982487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29180
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42944096-A-G