33477178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31676111-T-G

33477186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31676101-T-C

33485004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658899-G-A

33485004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658899-G-C

33485004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658899-G-T

33485010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658893-G-A

33485010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658893-G-T

33485014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658889-G-A

33485014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658889-G-T

http://identifiers.org/hco/8/GRCh38#33485015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31658888-C-A

33485015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658888-C-T

http://identifiers.org/hco/8/GRCh38#33485017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31658886-C-A

33485017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658886-C-T

http://identifiers.org/hco/8/GRCh38#33485064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31658845-A-C

33485064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658845-A-T

33485067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658842-G-A

33485067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658842-G-T

http://identifiers.org/hco/8/GRCh38#33485070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31658839-A-C

33485070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658839-A-T

33485080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658829-T-C

33485159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658753-T-A

33485159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658753-T-G

33485184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658728-T-C

33485184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658728-T-G

33485199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658713-C-G

33485199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658713-C-T

33485227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658684-T-A

33485319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658592-C-G

33485347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658566-G-A

33485347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658566-G-T

33485385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658528-T-A

33485385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658528-T-C

33485385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658528-T-G

33485472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658476-T-C

http://identifiers.org/hco/8/GRCh38#33485573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31658396-C-A

33485573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658396-C-T

http://identifiers.org/hco/8/GRCh38#33485597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31658382-C-A

33485597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658382-C-T

33485619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658355-C-T

33485664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658312-C-T

33485698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658273-T-C

33485774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658188-G-A

33486044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31658010-T-C

33486812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31657820-C-T

33486829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31657803-T-C

33486948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31657701-C-T

33487177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31657498-T-C

http://identifiers.org/hco/8/GRCh38#33487192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31657483-C-A

http://identifiers.org/hco/8/GRCh38#33488470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31656696-C-A

33488470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656696-C-T

33488471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656695-C-G

http://identifiers.org/hco/8/GRCh38#33488503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31656675-C-A

33488503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656675-C-G

33488679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656520-G-A

33488679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656520-G-C

33488679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656520-G-T

33488803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656395-G-A

33488858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656351-G-C

33488858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656351-G-T

33488938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656286-T-C

33488944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656282-A-G

33488958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656268-C-T

http://identifiers.org/hco/8/GRCh38#33489275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31656014-A-C

33489275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656014-A-G

http://identifiers.org/hco/8/GRCh38#33489283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31656006-C-A

33489283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656006-C-G

33489283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31656006-C-T

http://identifiers.org/hco/8/GRCh38#33489405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31655922-C-A

33489910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31655365-C-T

33489911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31655364-G-A

33489922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31655353-C-G

33490142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31654957-G-A

33490142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31654957-G-T

33490150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31654949-G-T

33490236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31654836-G-A

33490236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31654836-G-T

33490255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31654831-G-T

33490428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31654694-G-A

33490461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31654660-T-A

33490461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31654660-T-C

33495404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31653248-A-G

33495404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31653248-A-T

http://identifiers.org/hco/8/GRCh38#33495460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31653202-C-A

33495460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31653202-C-T

33495639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31653034-G-T

33496524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31651947-G-T

33496529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31651942-A-T

33496703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 31651783-G-T

33496747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31651742-T-C

33496749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 31651740-T-A

33496749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 31651740-T-C

http://identifiers.org/hco/8/GRCh38#33496764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31651722-C-A

33496768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31651712-C-T

33496788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31651690-T-A

33496799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31651679-A-T

http://identifiers.org/hco/8/GRCh38#33496812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31651668-C-A

33496812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31651668-C-T

33497098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31650979-A-G

33497151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31650928-A-G

33497239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 31650843-G-A

33497239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 31650843-G-T

33497342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31650742-A-G

33497343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31650741-A-G

33498349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31650683-T-C

33498349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31650683-T-G

33498363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31650669-G-A

33498363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31650669-G-C

33498363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31650669-G-T

33498390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31650643-A-T

http://identifiers.org/hco/8/GRCh38#33498424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31650611-C-A

33498424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 31650611-C-T

33498508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 31650536-C-T

http://identifiers.org/hco/8/GRCh38#33498723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#31650388-C-A

33498723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31650388-C-T

33498814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31650296-G-A

33498814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31650296-G-T

33498845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31650268-T-C

http://identifiers.org/hco/8/GRCh38#33498975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#31650188-A-C

33498975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31650188-A-T

http://identifiers.org/hco/8/GRCh38#33499060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#31650118-C-A

33499060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31650118-C-T

33499111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31650067-C-T

33499124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31650054-A-G

http://identifiers.org/hco/8/GRCh38#33499160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#31650018-A-C

33499222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31649963-A-G

33499254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31649931-T-C

33499256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 31649929-G-A

http://identifiers.org/hco/8/GRCh38#33499296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#31649889-C-A

33499397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31649800-G-A

33499397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31649800-G-T

33499491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31649761-T-C

33499521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31649734-T-A

http://identifiers.org/hco/8/GRCh38#33499584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#31649669-A-C

33499660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31649595-G-A

33499660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31649595-G-T

33499716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31649586-T-G

33499743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31649566-A-G

33499839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31649473-T-C

33500065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31649164-T-C

33500148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31648987-A-G

33500151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31648984-G-A

33500151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31648984-G-T

33500407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31648702-T-A

http://identifiers.org/hco/8/GRCh38#33500638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#31648501-C-A

33500638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31648501-C-G

33500638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31648501-C-T

33500736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31648334-G-T

33503230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31646103-A-G

33503314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31646058-G-A

33503314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31646058-G-T

33503408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31645983-G-C

http://identifiers.org/hco/8/GRCh38#33503561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#31645815-A-C

33503561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31645815-A-G

33503641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31645770-G-A

33503647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31645764-G-A

33503647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31645764-G-T

33503648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31645763-T-A

33503883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31645592-T-C

33503883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31645592-T-G

33503936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 31645539-C-T

33504042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31645436-C-G

33504042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31645436-C-T

33504058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31645420-A-G

33504158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31645367-G-A

33505366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31644842-C-G

33507036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31644511-T-C

33507070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31644478-G-A

33507109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31644439-G-A

33507109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31644439-G-T

33507190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31644368-G-T

33507339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31644222-G-A

33507339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31644222-G-T

http://identifiers.org/hco/8/GRCh38#33509608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#31643900-C-A

33509609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31643899-A-G

33509609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31643899-A-T

33509669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31643836-A-G

33509709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31643754-T-C

33509824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: synonymous variant
orthologous variants: 31643643-T-A

33509824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: synonymous variant
orthologous variants: 31643643-T-C

33509824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: synonymous variant
orthologous variants: 31643643-T-G

33509942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron variant
orthologous variants: 31643525-T-A

33509942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron variant
orthologous variants: 31643525-T-C

33510009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron variant
orthologous variants: 31643469-G-A

33510009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron variant
orthologous variants: 31643469-G-T

33510034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: intron variant
orthologous variants: 31643429-T-A

http://identifiers.org/hco/8/GRCh38#33512019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/8/GRCm39#31641473-C-A

33512033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense variant
orthologous variants: 31641459-C-G

33512033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense variant
orthologous variants: 31641459-C-T

33512357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense variant
orthologous variants: 31641138-G-A

http://identifiers.org/hco/8/GRCh38#33512462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#31641027-A-C

33512462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense variant
orthologous variants: 31641027-A-G

33512489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense variant
orthologous variants: 31640997-G-C

33512491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: synonymous variant
orthologous variants: 31640995-C-T

33512509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: synonymous variant
orthologous variants: 31640977-G-A

33512597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense variant
orthologous variants: 31640892-G-C

http://identifiers.org/hco/8/GRCh38#33512598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#31640891-C-A

33512598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense variant
orthologous variants: 31640891-C-G

33512598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: missense variant
orthologous variants: 31640891-C-T

33512613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: undefined
orthologous variants: 31640876-T-C

33512621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5 prime UTR variant
orthologous variants: 31640871-T-G

33512622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5 prime UTR variant
orthologous variants: 31640870-G-A

33512624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5 prime UTR variant
orthologous variants: 31640868-A-G

33512628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5 prime UTR variant
orthologous variants: 31640864-C-G

33512628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5 prime UTR variant
orthologous variants: 31640864-C-T

http://identifiers.org/hco/8/GRCh38#33512641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#31640850-C-A

33512641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5 prime UTR variant
orthologous variants: 31640850-C-G

33512641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5 prime UTR variant
orthologous variants: 31640850-C-T

http://identifiers.org/hco/8/GRCh38#33512643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#31640837-C-A

33512643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5 prime UTR variant
orthologous variants: 31640837-C-G

33512652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5 prime UTR variant
orthologous variants: 31640828-A-G

33512682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5 prime UTR variant
orthologous variants: 31640789-G-A

33512682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5 prime UTR variant
orthologous variants: 31640789-G-T

http://identifiers.org/hco/8/GRCh38#33512848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#31640577-C-A

33512848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31640577-C-G

33512898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31640545-G-A

33512898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31640545-G-C

33512898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31640545-G-T

33513077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31640398-G-A

33513077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31640398-G-C

33513176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 31640291-G-A

33513176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26262
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 31640291-G-T