102233992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96743999-A-G

http://identifiers.org/hco/5/GRCh38#102234201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96744209-C-A

http://identifiers.org/hco/5/GRCh38#102234309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96744316-C-A

102234312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96744319-A-G

102234322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96744329-G-T

102234569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96744543-A-G

102234627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96744594-C-T

http://identifiers.org/hco/5/GRCh38#102234706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96744672-C-A

102234891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96744838-G-T

102234937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96744884-T-A

http://identifiers.org/hco/5/GRCh38#102234968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96744913-C-A

102235074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96745021-G-A

102235074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96745021-G-T

102235216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96745178-A-G

102235929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96745613-A-G

102235959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96745641-C-T

102236028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96745710-T-G

http://identifiers.org/hco/5/GRCh38#102236054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96745751-C-A

102236214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96745913-A-G

102236256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96745958-T-C

102236296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96745994-A-G

102236471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96746291-A-G

102236521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96746373-G-A

102236521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96746373-G-C

102236521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96746373-G-T

102236552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96746404-T-G

102236771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96746595-T-C

102236798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96746622-T-C

102236806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96746630-T-A

102236806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96746630-T-G

102236853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 3 prime UTR variant
orthologous variants: 96746667-C-T

102236894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: synonymous variant
orthologous variants: 96746708-T-G

102236939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: missense variant
orthologous variants: 96746753-A-T

102237036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96746850-T-A

102237036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96746850-T-C

102237036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96746850-T-G

102237064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96746914-G-A

102237064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96746914-G-T

102237072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96746928-T-A

102237083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96746939-A-G

102237187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96747080-T-A

102237253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96747163-T-C

102237256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96747166-T-G

102237264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96747174-G-A

102237267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96747177-T-C

102237277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96747189-T-A

102237576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96747447-C-T

http://identifiers.org/hco/5/GRCh38#102237851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96747696-A-C

102238105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96747906-A-G

http://identifiers.org/hco/5/GRCh38#102238863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96748491-C-A

102238950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96748667-G-A

http://identifiers.org/hco/5/GRCh38#102239123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96748830-C-A

102239131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96748838-T-C

102239156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96748863-T-C

http://identifiers.org/hco/5/GRCh38#102239161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96748868-A-C

102239175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96748881-T-C

http://identifiers.org/hco/5/GRCh38#102239387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96749044-C-A

102239387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 96749044-C-T

102239440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96749095-T-C

102239492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96749155-G-T

102239515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96749180-T-A

http://identifiers.org/hco/5/GRCh38#102239535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96749200-A-C

http://identifiers.org/hco/5/GRCh38#102239537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96749202-A-C

102239537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96749202-A-G

102239537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96749202-A-T

102239601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96749266-T-C

102239662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96750706-T-C

102239844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96750909-T-C

102240506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96751168-A-G

http://identifiers.org/hco/5/GRCh38#102240595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96751274-C-A

102240595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96751274-C-G

102240595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96751274-C-T

102240633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96751316-G-T

102240816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96751518-G-T

102240825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96751527-G-A

102240825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96751527-G-T

102241621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96752262-C-G

http://identifiers.org/hco/5/GRCh38#102246750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96756080-A-C

102246866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96756189-G-A

102247029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96756329-C-T

102247062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96756358-A-G

102247165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96756441-A-G

http://identifiers.org/hco/5/GRCh38#102247173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96756448-C-A

102247212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96756476-G-A

http://identifiers.org/hco/5/GRCh38#102247519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96756746-C-A

http://identifiers.org/hco/5/GRCh38#102247535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96756766-A-C

102247544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96756774-T-A

http://identifiers.org/hco/5/GRCh38#102247584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96756813-C-A

102247584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96756813-C-T

102249415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96759497-T-A

102249430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96759512-G-A

102249475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96759559-A-G

102249624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96759698-G-A

102249647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: synonymous variant
orthologous variants: 96759720-C-T

102249733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: stop gained
orthologous variants: 96759809-G-A

102249752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: synonymous variant
orthologous variants: 96759828-A-G

102249752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: missense variant
orthologous variants: 96759828-A-T

http://identifiers.org/hco/5/GRCh38#102249785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96759861-A-C

102249827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96759907-A-G

102249839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96759919-T-C

http://identifiers.org/hco/5/GRCh38#102249848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96759928-C-A

102249848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96759928-C-T

http://identifiers.org/hco/5/GRCh38#102249919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96759981-A-C

102250384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96760612-T-C

102250431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96760655-T-G

102250449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96760672-A-G

102250566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96760794-A-G

102250623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96760833-G-A

102251342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96761468-T-C

102251407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96761529-G-C

102251586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96761625-T-C

102251997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96762008-G-C

102252255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96762344-C-T

102252724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96762729-T-C

102255549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96763071-A-G

http://identifiers.org/hco/5/GRCh38#102255739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96763300-A-C

102255852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96763410-G-C

102256664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96763813-A-G

102257557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96765025-A-T

102257865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96765088-T-C

102257897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96765118-T-C

102257901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96765122-G-A

102258049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: synonymous variant
orthologous variants: 96765285-T-A

102258049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: synonymous variant
orthologous variants: 96765285-T-C

102258124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96765358-A-G

102258128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96765362-T-C

102258379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96765717-G-A

102258473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96765811-A-G

102258614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766218-T-G

102260001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766691-C-T

102260107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766796-T-A

102260107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766796-T-C

102260111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766800-T-A

102260111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766800-T-C

102260111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766800-T-G

102260114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766808-T-A

102260114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766808-T-C

102260118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766812-T-A

102260118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766812-T-G

102260128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766822-T-A

102260128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766822-T-C

102260161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766844-T-C

102260182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766865-G-A

102260182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766865-G-T

102260188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766871-G-A

102260188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766871-G-C

102260188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96766871-G-T

http://identifiers.org/hco/5/GRCh38#102260924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96768228-A-C

102260932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96768236-T-C

102261516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96768507-G-A

102261516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96768507-G-T

102261616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96768606-A-G

102261692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96768670-T-G

102261727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96768701-A-T

102261818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96768764-A-G

102261872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96768815-T-A

102261872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96768815-T-G

102261904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 96768847-A-G

102262097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96769033-A-G

102262097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96769033-A-T

102262165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96769099-T-C

102262274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96769450-T-C

102262413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96769583-G-T

102263481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770019-A-T

102263506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770030-C-T

102263559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770078-A-G

http://identifiers.org/hco/5/GRCh38#102263586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96770103-C-A

102263627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770138-G-T

102263734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: synonymous variant
orthologous variants: 96770229-T-C

102263776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: synonymous variant
orthologous variants: 96770271-G-A

102263787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 96770282-G-T

http://identifiers.org/hco/5/GRCh38#102263805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96770300-A-C

http://identifiers.org/hco/5/GRCh38#102263838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96770332-C-A

102263838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770332-C-T

102263846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770343-G-A

102263846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770343-G-T

http://identifiers.org/hco/5/GRCh38#102263879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96770373-C-A

102263879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770373-C-G

102263879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770373-C-T

http://identifiers.org/hco/5/GRCh38#102263893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96770389-A-C

102263893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770389-A-G

102263896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770392-A-G

http://identifiers.org/hco/5/GRCh38#102263931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96770455-A-C

102263966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770490-C-T

102264056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770581-T-C

102264147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96770650-T-A

102270375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96771960-T-G

102270382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96771967-G-A

102270513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96772076-A-G

102270519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96772082-T-A

102270519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96772082-T-C

102270520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96772083-G-A

102270520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96772083-G-T

102270550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96772106-T-C

102270587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96772150-T-A

102270587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96772150-T-C

102270598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96772162-T-C

http://identifiers.org/hco/5/GRCh38#102270613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96772190-A-C

102270631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: synonymous variant
orthologous variants: 96772208-G-A

102270631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: synonymous variant
orthologous variants: 96772208-G-C

102270631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: synonymous variant
orthologous variants: 96772208-G-T

102270703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: synonymous variant
orthologous variants: 96772280-T-C

102270703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: synonymous variant
orthologous variants: 96772280-T-G

102270804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 96772378-T-G

http://identifiers.org/hco/5/GRCh38#102274269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96774639-C-A

102274303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96774673-C-T

102282820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96787517-T-C

102282956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96787653-G-C

http://identifiers.org/hco/5/GRCh38#102282975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96787671-A-C

102283075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96787767-T-C

102283106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96787819-T-C

102283417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96788111-G-C

102283584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96788274-G-A

102283584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96788274-G-T

102283636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96788346-T-A

102283636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96788346-T-G

102286890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96791575-A-G

102289384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96793253-C-T

102289405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96793271-T-C

102289417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96793283-A-G

102289492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96793775-T-C

102289499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96793782-C-T

102289696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96793962-T-G

102289784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96794043-T-C

102289829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96794087-C-G

102289829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96794087-C-T

102289951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96794208-T-C

102290489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96794620-A-G

102290540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96794684-T-A

102291123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96795251-A-G

102291129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96795257-G-T

http://identifiers.org/hco/5/GRCh38#102291290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96795393-A-C

102291332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96795439-T-C

102291337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96795444-A-G

102291635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96795735-A-T

102291664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96795764-T-C

102291845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96795905-G-C

102291883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96795962-G-A

102292510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96796641-T-C

102292682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96796961-A-G

102292785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96797055-T-C

102293222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96797570-G-A

102293222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96797570-G-T

102293282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96797636-T-C

http://identifiers.org/hco/5/GRCh38#102294448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#96798036-C-A

102294448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96798036-C-T

102294451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96798039-T-C

102294451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96798039-T-G

102294647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96798210-A-G

102294772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 96798322-A-G

102294793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 96798354-T-C

102294810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96798371-A-G

102295291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96798845-T-C

102295421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96798971-T-C

102295464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96799026-C-T

102295468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron variant
orthologous variants: 96799030-C-T

102295615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 96799164-A-G

102295761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron_variant, undefined
orthologous variants: 96799313-G-A

http://identifiers.org/hco/5/GRCh38#102295813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#96799384-C-A

102295813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron_variant, undefined
orthologous variants: 96799384-C-T

http://identifiers.org/hco/5/GRCh38#102295824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#96799405-C-A

102295824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron_variant, undefined
orthologous variants: 96799405-C-G

102295824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron_variant, undefined
orthologous variants: 96799405-C-T

102295877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron_variant, undefined
orthologous variants: 96799457-G-A

102295877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron_variant, undefined
orthologous variants: 96799457-G-T

http://identifiers.org/hco/5/GRCh38#102295878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#96799458-C-A

102296136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 96799708-T-C

102296272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 5 prime UTR variant
orthologous variants: 96799845-G-A

102296272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 5 prime UTR variant
orthologous variants: 96799845-G-C

102296272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23612
most severe consequence: 5 prime UTR variant
orthologous variants: 96799845-G-T