http://identifiers.org/hco/3/GRCh38#45082377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122999743-C-A

45082410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122999786-G-A

45082615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 122999975-A-G

45082682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000040-T-C

45082703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000056-T-A

45082703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000056-T-C

45082710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000063-T-C

http://identifiers.org/hco/3/GRCh38#45082767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123000098-C-A

45083165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000233-A-G

45083167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000235-T-G

45083199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000253-G-A

45083199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000253-G-T

45083286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000360-C-T

45083412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000457-A-G

45083414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000459-G-T

45083448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000486-A-G

http://identifiers.org/hco/3/GRCh38#45083499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123000532-C-A

http://identifiers.org/hco/3/GRCh38#45083554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123000562-C-A

45084206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000785-T-C

45084207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123000786-G-T

45084531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123001108-G-A

45084531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123001108-G-T

45084674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123001223-G-A

45084697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123001244-G-A

45084697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123001244-G-T

45084797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123001550-G-T

http://identifiers.org/hco/3/GRCh38#45085062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#123001790-C-A

45085062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 123001790-C-G

45085062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 123001790-C-T

45085082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 123001810-A-G

45085095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123001823-A-G

http://identifiers.org/hco/3/GRCh38#45085111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123001839-C-A

45085124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123001852-T-G

45085154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 123001896-T-C

45085311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 123002247-G-T

45085312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 123002248-T-G

45085313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 123002249-T-G

45085331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123002275-G-A

45085331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123002275-G-T

45085384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123002327-G-A

45085384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123002327-G-T

http://identifiers.org/hco/3/GRCh38#45085389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123002332-C-A

http://identifiers.org/hco/3/GRCh38#45085588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123002517-C-A

45085588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123002517-C-T

45085598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3 prime UTR variant
orthologous variants: 123002527-T-G

45085680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 123002610-A-G

45085684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 123002614-T-C

http://identifiers.org/hco/3/GRCh38#45085752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123002682-A-C

45085762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: missense variant
orthologous variants: 123002692-C-G

45085762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: missense variant
orthologous variants: 123002692-C-T

45085773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 123002703-C-T

45086151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123003044-G-A

45086151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123003044-G-T

45086174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123003067-G-T

45086237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123003125-T-C

http://identifiers.org/hco/3/GRCh38#45086709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123003581-C-A

45088544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123004241-T-C

http://identifiers.org/hco/3/GRCh38#45088998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123004741-C-A

45088998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123004741-C-G

45089020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123004764-A-G

45089065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 123004811-A-G

45089130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, missense_variant
orthologous variants: 123004873-T-C

45089163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123004904-G-A

45089163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123004904-G-T

45089204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123004944-T-A

45089204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123004944-T-G

45089206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123004946-A-G

45089279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123004968-G-A

45089280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123004969-G-A

45089280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123004969-G-T

45089476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123005113-T-C

45089476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123005113-T-G

45089492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123005128-G-A

45089525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123005167-C-T

45089731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123005529-T-C

45089771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123005556-C-G

45089819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123005601-C-G

http://identifiers.org/hco/3/GRCh38#45089926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123005699-A-C

45089926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123005699-A-T

45089948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123005721-A-G

45090039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123005787-G-C

45090844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123006478-G-A

45090918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123006549-T-C

45090974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123006603-G-A

http://identifiers.org/hco/3/GRCh38#45091065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123006638-C-A

45091065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123006638-C-G

45091065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123006638-C-T

45091078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123006651-A-G

http://identifiers.org/hco/3/GRCh38#45091099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123006672-C-A

45091111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123006684-T-C

45091111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123006684-T-G

45091145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123006724-T-A

45091145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123006724-T-C

http://identifiers.org/hco/3/GRCh38#45091156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123006736-A-C

45091156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123006736-A-G

http://identifiers.org/hco/3/GRCh38#45091174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123006754-C-A

45091174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 123006754-C-T

45091183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: synonymous variant
orthologous variants: 123006763-T-C

http://identifiers.org/hco/3/GRCh38#45091462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123007042-C-A

45091549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123007129-G-A

45091549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123007129-G-T

45091573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123007155-T-C

45091584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123007165-A-G

45091584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123007165-A-T

http://identifiers.org/hco/3/GRCh38#45091595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123007176-A-C

http://identifiers.org/hco/3/GRCh38#45091615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123007195-C-A

45091615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123007195-C-G

45091615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123007195-C-T

45091632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123007207-G-T

http://identifiers.org/hco/3/GRCh38#45091634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123007209-C-A

45091634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123007209-C-T

45091666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123007241-T-A

45091666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123007241-T-C

45092227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123007818-A-T

45092307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, undefined
orthologous variants: 123007877-C-G

45092307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, undefined
orthologous variants: 123007877-C-T

45092978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123008650-C-T

45093291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: missense variant
orthologous variants: 123009064-A-G

45093291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: missense variant
orthologous variants: 123009064-A-T

http://identifiers.org/hco/3/GRCh38#45093323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123009096-C-A

45093323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: synonymous variant
orthologous variants: 123009096-C-T

http://identifiers.org/hco/3/GRCh38#45093673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123009446-C-A

45093740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123009519-G-T

http://identifiers.org/hco/3/GRCh38#45093828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123009554-C-A

45093828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123009554-C-T

45095295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123011165-G-T

45095556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: missense variant
orthologous variants: 123011439-A-G

45095558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: synonymous variant
orthologous variants: 123011441-G-A

45095558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: stop gained
orthologous variants: 123011441-G-T

45095627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123011509-G-A

45095627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123011509-G-T

http://identifiers.org/hco/3/GRCh38#45095628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123011510-C-A

45109922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123011823-C-T

http://identifiers.org/hco/3/GRCh38#45110069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123011936-A-C

45110069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123011936-A-G

http://identifiers.org/hco/3/GRCh38#45110122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123012020-A-C

45110146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123012051-G-A

45110146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123012051-G-T

45110212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123012117-T-A

45110346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 123012420-G-C

45110346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 123012420-G-T

45110795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: synonymous variant
orthologous variants: 123012844-G-C

45110795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: synonymous variant
orthologous variants: 123012844-G-T

45110930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123012974-A-G

45110999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123013029-T-C

http://identifiers.org/hco/3/GRCh38#45111027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123013057-C-A

45111027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123013057-C-T

45111028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123013058-G-A

45111081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123013105-C-G

45111081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123013105-C-T

http://identifiers.org/hco/3/GRCh38#45111957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123013947-A-C

45111957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123013947-A-G

45111957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123013947-A-T

45111983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123013977-G-A

45111983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123013977-G-T

45112006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123014009-T-C

http://identifiers.org/hco/3/GRCh38#45112021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123014025-C-A

45112021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123014025-C-T

http://identifiers.org/hco/3/GRCh38#45112027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123014031-C-A

45112096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: synonymous variant
orthologous variants: 123014131-G-A

45112267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: synonymous variant
orthologous variants: 123014302-G-A

45112267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: missense variant
orthologous variants: 123014302-G-C

http://identifiers.org/hco/3/GRCh38#45112486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123014523-C-A

45112538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123014568-T-C

45112635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123014614-T-G

45113168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123015455-T-A

45113240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123015517-G-A

45113710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123016798-C-T

45113838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123016926-G-A

45114118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123017316-G-C

http://identifiers.org/hco/3/GRCh38#45114396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123017575-C-A

45114873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123017725-G-T

45118065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123018343-T-C

45118318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123018909-A-G

45118334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123018925-T-G

45118553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123019127-G-A

45118553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123019127-G-C

http://identifiers.org/hco/3/GRCh38#45118668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123019240-C-A

45118674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123019246-G-T

45121169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123027602-C-T

45121284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123027774-A-G

45121498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123027991-T-A

45121756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123028237-T-C

45121995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123028425-T-C

45123420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123029749-G-A

45123469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123029799-T-C

45123686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123029982-A-G

45123686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123029982-A-T

45123712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123030009-T-A

45123893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123030409-G-A

45124006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123030502-C-T

45124058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123030551-A-G

45124173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123030669-C-T

45124265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123030708-T-C

45124311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123030748-T-C

45124314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123030751-C-T

45124382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123030816-A-G

45124451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123030880-A-G

45125293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123031497-C-T

45125480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123031624-T-C

45125525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123031670-G-A

45125569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123031717-T-C

http://identifiers.org/hco/3/GRCh38#45125598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123031746-C-A

45125598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123031746-C-T

45125690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123031833-T-C

45125777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123031915-T-C

45125784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123031922-A-G

45127023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123032428-C-T

http://identifiers.org/hco/3/GRCh38#45127688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123032813-A-C

45129419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123033015-G-A

45129419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123033015-G-C

45129618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123033202-G-A

45129618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123033202-G-C

45135554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123033386-C-T

45135689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123033508-C-T

45136679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123034235-T-A

45136941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123034627-T-C

45137822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123035579-T-C

45137843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123035599-G-A

45138310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123036009-G-A

45139568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123036787-T-C

45139591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123036809-G-C

45139603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123036827-G-A

45139603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123036827-G-T

45139632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123036857-G-A

45140095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123037262-C-T

45140150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, undefined
orthologous variants: 123037314-T-C

45140187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123037346-A-T

45141224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123040510-C-T

45141438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123040706-G-A

45141692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123041375-G-C

45141715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123041393-T-C

45141738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123041410-C-T

45144176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123042504-T-C

45144438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123042697-G-A

http://identifiers.org/hco/3/GRCh38#45144791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123043543-C-A

45144791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123043543-C-G

45145280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123044169-C-T

45145310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123044201-C-G

45145316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123044207-C-T

45145381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123044266-T-A

45145381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123044266-T-C

45145622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123044468-T-C

45145638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123044474-G-T

http://identifiers.org/hco/3/GRCh38#45145673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123044509-C-A

45145685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123044521-A-G

45145686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123044522-G-A

45145811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123044632-C-T

45145864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, undefined
orthologous variants: 123044669-G-A

45145923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron_variant, undefined
orthologous variants: 123044710-C-T

45146157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: intron variant
orthologous variants: 123044873-T-C

http://identifiers.org/hco/3/GRCh38#45146252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123044939-C-A

45146252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 123044939-C-T

http://identifiers.org/hco/3/GRCh38#45146257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#123044944-C-A

45146257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 123044944-C-T

http://identifiers.org/hco/3/GRCh38#45146337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123045030-C-A

45146337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 123045030-C-T

45146455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24357
most severe consequence: 5 prime UTR variant
orthologous variants: 123045141-T-C