26308708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30398588-C-G

26308839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30398750-G-T

26308871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30398790-G-C

26308871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30398790-G-T

26309476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30399998-G-A

26309476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30399998-G-T

26309500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400017-T-C

26309593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400108-T-A

26309651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400164-G-T

26309826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400312-G-T

26309846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400332-G-A

26309846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400332-G-T

26310014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400471-C-T

26310113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 30400565-A-G

26310167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400621-G-A

26310178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400632-T-A

26310178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400632-T-G

26310235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 30400687-G-A

http://identifiers.org/hco/2/GRCh38#26310244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30400696-A-C

26310247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400699-G-A

26310262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400708-G-A

26310280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400726-G-T

26310313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400771-G-C

26310313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400771-G-T

26310377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400860-T-A

26310380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30400863-A-G

26310650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30401192-A-G

26310803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30401345-C-G

26310863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30401405-C-T

http://identifiers.org/hco/2/GRCh38#26310975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30401517-C-A

26310975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30401517-C-G

http://identifiers.org/hco/2/GRCh38#26311097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30401639-C-A

26311097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30401639-C-T

26311200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30401742-G-A

26311200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30401742-G-T

26311223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30401765-C-T

26311238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30401780-T-C

26311238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30401780-T-G

26311298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30401840-G-A

26311298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30401840-G-C

26311325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30401867-C-T

26311359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30401901-C-G

26311416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30401958-G-A

26311511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30402050-G-A

26311519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 30402058-G-A

26311625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30402164-C-T

26311675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30402214-C-G

26311675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30402214-C-T

26311694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30402233-G-C

26311796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30402335-T-C

26311901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30402440-C-T

26311943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 30402482-G-T

26311955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30402494-T-A

26311955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30402494-T-C

26312194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30402712-G-T

26312196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30402714-A-G

http://identifiers.org/hco/2/GRCh38#26312216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30402731-C-A

26312216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30402731-C-G

26312216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30402731-C-T

26312334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30402840-T-G

26312674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30403139-C-T

http://identifiers.org/hco/2/GRCh38#26312845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30403267-A-C

26312854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30403275-T-G

http://identifiers.org/hco/2/GRCh38#26312956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30403374-C-A

26312956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30403374-C-T

26313133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30403653-C-T

26313222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30403785-C-T

http://identifiers.org/hco/2/GRCh38#26313224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30403787-C-A

26313229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30403791-C-T

26313250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30403817-G-A

26313250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30403817-G-T

26313330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30403924-G-A

26313330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30403924-G-T

26313410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30404048-A-T

http://identifiers.org/hco/2/GRCh38#26313420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30404058-C-A

26313420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30404058-C-T

26313473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 30404111-G-T

26313614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30404249-T-C

26313668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30404303-G-A

26314012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30404640-A-G

http://identifiers.org/hco/2/GRCh38#26314027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30404655-C-A

26314027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30404655-C-T

26314038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30404667-G-T

26314050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30404679-T-G

26314270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30405350-G-A

26314270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30405350-G-T

26314766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30405794-T-C

26314868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30405889-A-G

26314868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30405889-A-T

26314913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30405937-G-A

26314913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30405937-G-T

http://identifiers.org/hco/2/GRCh38#26314919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30405943-C-A

26315429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407056-G-A

26315429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407056-G-T

26315453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407080-G-C

26315453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407080-G-T

26315463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407146-G-A

26315463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407146-G-T

26315561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407276-C-G

26315561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407276-C-T

http://identifiers.org/hco/2/GRCh38#26315712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30407427-C-A

26315712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30407427-C-T

26315725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407440-T-A

26315725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407440-T-C

26315755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407471-G-A

http://identifiers.org/hco/2/GRCh38#26315849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30407533-C-A

26315850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407534-T-C

http://identifiers.org/hco/2/GRCh38#26315879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30407561-C-A

26315920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407599-G-A

26315965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407641-G-A

26316142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407785-G-A

26316142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407785-G-T

26316147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407790-T-C

26316148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407792-T-C

26316154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407798-A-T

26316164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407820-G-A

26316164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407820-G-T

26316226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407905-A-G

26316255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30407935-A-G

http://identifiers.org/hco/2/GRCh38#26316564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30408194-C-A

26316564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408194-C-G

26316564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408194-C-T

26316578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408207-C-T

26316586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408215-G-T

26316595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408224-A-T

26316611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408240-C-T

26316655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408285-G-A

26316784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408379-A-G

26316966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30408536-C-G

26317145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408713-C-T

26317313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408896-A-G

26317329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408939-G-A

26317329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408939-G-C

26317362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30409037-G-T

26317369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30409051-G-T

26317400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30409125-G-A

26317400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30409125-G-T

http://identifiers.org/hco/2/GRCh38#26317451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30409291-C-A

http://identifiers.org/hco/2/GRCh38#26317471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30409314-C-A

26317471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30409314-C-T

http://identifiers.org/hco/2/GRCh38#26317480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30409323-C-A

26317480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30409323-C-T

26317549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30409386-G-A

26317549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30409386-G-T

26317660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30409507-G-T

26317673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30409520-C-T

26317679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30409526-G-A

26317700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30409546-G-T

26317724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30409570-G-T

26317864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 30409719-G-A

26317864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 30409719-G-T

http://identifiers.org/hco/2/GRCh38#26318158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30409876-A-C

26318158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30409876-A-G

26318472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410178-T-C

26318487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410193-A-G

26318727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410421-A-G

26318804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410496-G-C

26318804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410496-G-T

26318846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410529-T-C

26318911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410557-G-A

26318911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410557-G-C

26318911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410557-G-T

26319097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410782-G-A

26319097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410782-G-C

26319097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410782-G-T

26319141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410824-G-T

26319154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410837-G-A

26319154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410837-G-T

26319155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410838-G-C

26319155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410838-G-T

26319193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410875-T-C

26319317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410975-G-A

26319317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30410975-G-T

26319432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30411092-C-T

26342236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30426716-C-T

26342375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30427185-T-C

26342420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30427231-T-C

26342572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30427366-T-G

26342729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30427608-G-A

http://identifiers.org/hco/2/GRCh38#26342757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30427644-A-C

26345370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437048-C-G

26345370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437048-C-T

http://identifiers.org/hco/2/GRCh38#26345659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30437277-A-C

26345659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437277-A-G

26345659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437277-A-T

26345747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437324-C-G

26345747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437324-C-T

26345772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437347-C-G

26345772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437347-C-T

26345926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437476-T-C

http://identifiers.org/hco/2/GRCh38#26346107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30437627-C-A

26346107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437627-C-T

26346316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437845-T-C

http://identifiers.org/hco/2/GRCh38#26346326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30437856-C-A

26346326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437856-C-T

26346435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 30437955-G-A

http://identifiers.org/hco/2/GRCh38#26346497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30438017-C-A

26346497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438017-C-G

26346497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438017-C-T

26346662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438176-G-A

26346662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438176-G-T

26346677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438191-G-A

26346677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438191-G-T

26346724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438236-G-T

http://identifiers.org/hco/2/GRCh38#26346746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30438259-C-A

26346746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438259-C-T

26346756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438269-G-A

26346756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438269-G-C

26346768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438281-G-T

26346787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438297-T-C

26346799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438309-G-A

26346799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438309-G-T

26346881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30438391-A-G

26347246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30438683-C-T

26347291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30438713-G-A

26347323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30438745-G-T

26347536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30438922-T-G

http://identifiers.org/hco/2/GRCh38#26347580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30438970-A-C

26347645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439018-C-T

26347939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439279-A-T

26348242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439602-T-G

26348428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439782-G-C

26348573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439922-C-T

26348577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439926-C-G

26348577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439926-C-T

26348631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439980-G-A

26348740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30440064-A-G

26348740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30440064-A-T

26349015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30440376-T-C

26349016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30440377-T-G

26349598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30440523-G-T

26349711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30440570-G-T

26350183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30440713-T-C

26353260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30442446-G-A

26353515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30443035-T-C

26359895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30450358-A-G

26359895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30450358-A-T

26359923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30450381-G-A

26359965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30450413-C-T

26360051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30450494-C-T

26360159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30450576-A-G

26363534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30452147-T-A

26363534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30452147-T-G

26363567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30452175-C-T

26363623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30452228-C-T

26364391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30452549-G-A

26364391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30452549-G-C

26364436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30452593-G-A

26364436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30452593-G-T

26364440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30452597-T-A

26364440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30452597-T-C

26364985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30453571-A-G

26365045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30453627-G-C

26365186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30453969-A-G

http://identifiers.org/hco/2/GRCh38#26365247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30454032-A-C

26365316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30454090-A-T

26367015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30457580-G-C

26367015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30457580-G-T

26367045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30457610-T-C

26367045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30457610-T-G

26367104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30457667-G-C

26367104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30457667-G-T

26367137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30457699-C-G

26367231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30457793-G-A

26367231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30457793-G-T

26367521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30458311-T-C

26367864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30458656-G-A

26367880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30458671-C-T

26368114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30458850-A-G

26368114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30458850-A-T

26368680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30459074-G-C

26368840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30459260-T-C

26369695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30459713-A-G

http://identifiers.org/hco/2/GRCh38#26373235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30460956-C-A

26373235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30460956-C-G

26373235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30460956-C-T

26373257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30460976-A-T

26373329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30461040-A-G

26373590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30461299-G-T

26374335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30462333-C-G

26374890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30462575-G-A

26374951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30462628-A-T

26375004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30462681-T-C

26375267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30462920-A-G

http://identifiers.org/hco/2/GRCh38#26375275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30462928-A-C

26375275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30462928-A-G

26375427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30463074-G-A

26375470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30463116-A-T

26375561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30463201-A-G

26375561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30463201-A-T

26381192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30465981-T-G

26381312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30466082-C-T

26381337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30466105-T-C

26381347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30466115-C-G

http://identifiers.org/hco/2/GRCh38#26381470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30466237-A-C

26381475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30466242-C-T

26381575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30466321-A-G

26381628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30466371-G-A

http://identifiers.org/hco/2/GRCh38#26382182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30467096-A-C

26382506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30467348-A-G

http://identifiers.org/hco/2/GRCh38#26382959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30467724-C-A

26382973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30467735-G-A

26383151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30467918-G-T

http://identifiers.org/hco/2/GRCh38#26383270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30468040-C-A

26383270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30468040-C-T

http://identifiers.org/hco/2/GRCh38#26383292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30468062-C-A

26383292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30468062-C-G

26383292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30468062-C-T

26383359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30468133-A-G

26383359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30468133-A-T

26385079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30469393-T-C

26386003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30469667-G-A

26386082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30469753-T-G

26386128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30470155-T-C

26386176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30470198-G-T

26386252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30470238-G-A

26386278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30470264-A-G

26386465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30470450-G-A

26386465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30470450-G-C

26386465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30470450-G-T

26386569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30470553-G-T

26386876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30470815-A-G

26388348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30471417-G-A

26388966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30471860-T-C

26388969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30471863-A-G

26388999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30471892-T-C

26389001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30471895-A-G

26389001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30471895-A-T

26389200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472080-G-A

26389434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472314-A-G

26389495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472375-T-C

26389531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472423-T-C

26389593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472482-G-A

26389593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472482-G-C

26389593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472482-G-T

26389616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472505-T-C

26389649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472531-G-A

26389692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472565-A-G

http://identifiers.org/hco/2/GRCh38#26389729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30472591-C-A

26389743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472605-A-G

http://identifiers.org/hco/2/GRCh38#26389746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30472608-A-C

26389815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472681-A-G

26389834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472698-C-T

26389845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472709-G-T

http://identifiers.org/hco/2/GRCh38#26389879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30472744-C-A

26389879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472744-C-T

26389959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472819-G-C

26389959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472819-G-T

26389994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472853-T-C

26390092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472946-A-G

26390141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30472995-C-G

26390146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30473000-G-T

26390181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30473035-A-G

26390298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30473148-T-G

26390360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30473210-C-T

26391123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30473869-G-A

26391123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30473869-G-T

26391212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30473961-A-G

26391355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30474102-G-A

http://identifiers.org/hco/2/GRCh38#26391356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30474103-C-A

26391356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30474103-C-T

http://identifiers.org/hco/2/GRCh38#26391592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30474302-C-A

26391731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30474377-G-T

26392210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30474774-A-G

26392317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30474781-G-A

26392389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30474826-G-A

http://identifiers.org/hco/2/GRCh38#26392537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30474951-C-A

26392537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30474951-C-G

26392537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30474951-C-T

http://identifiers.org/hco/2/GRCh38#26392539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30474953-C-A

26392539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30474953-C-T

26392569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30474982-G-A

26392569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30474982-G-C

26392749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30475147-T-C

26393175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30475426-A-G

26393212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30475463-G-T

http://identifiers.org/hco/2/GRCh38#26393280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30475529-C-A

26393280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30475529-C-T

26393331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30475577-T-C

26393331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30475577-T-G

http://identifiers.org/hco/2/GRCh38#26393465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30475698-C-A

26393465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30475698-C-T

26393539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30475766-G-T

26393560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30475790-A-T

26393674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30475904-T-C

26393771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30475983-G-T

26393877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30476087-G-T

26393886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30476093-T-C

26394451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30476171-G-T

26394494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30476197-T-C

26394676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30476357-G-T

26394724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30476395-G-A

26394789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30476454-A-G

26394826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30476491-G-T

http://identifiers.org/hco/2/GRCh38#26395031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30476689-A-C

http://identifiers.org/hco/2/GRCh38#26395077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30476725-C-A

26395104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30476739-C-G

26395157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30476792-C-T

26395235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30476861-G-T

26395299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30476924-T-C

26395415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30477021-G-C

http://identifiers.org/hco/2/GRCh38#26395466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30477074-C-A

http://identifiers.org/hco/2/GRCh38#26395467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30477075-A-C

26395467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30477075-A-G

26395477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30477077-G-T

26395496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30477096-G-T

26395639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29361
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30477228-G-A