http://identifiers.org/hco/10/GRCh38#104353678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47926023-C-A

http://identifiers.org/hco/10/GRCh38#104353709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47926054-C-A

http://identifiers.org/hco/10/GRCh38#104353752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#47926101-C-A

104353752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: 47926101-C-T

104353788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: 47926138-G-A

104353788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: 47926138-G-C

104353788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: 47926138-G-T

104353854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47926223-G-C

104353854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47926223-G-T

104354011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: 47926382-A-G

104354057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47926419-G-A

104354057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47926419-G-T

104354528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47926748-T-C

104354836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47927044-C-G

104354836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47927044-C-T

104354890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47927097-G-A

104354890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47927097-G-T

http://identifiers.org/hco/10/GRCh38#104354897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47927104-A-C

104354897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47927104-A-T

104354980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47927168-C-T

104355192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47927337-A-T

104355871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47927753-T-C

104356041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47927913-C-T

104356318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47928189-A-G

http://identifiers.org/hco/10/GRCh38#104356338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47928209-C-A

104356357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47928228-G-C

104356498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47928368-C-T

104356882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47928856-T-C

104358109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47929279-A-G

104358109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47929279-A-T

104358199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47929361-A-G

104358226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47929388-G-A

104358232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47929394-A-T

104358360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 47929569-T-C

104358493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47929702-T-C

104358499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47929708-T-C

104358629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47929838-G-A

http://identifiers.org/hco/10/GRCh38#104358676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47929881-A-C

104358742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47929934-T-G

104358752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47929944-T-G

http://identifiers.org/hco/10/GRCh38#104358828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47930014-A-C

104358853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47930048-A-G

104359088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47930548-C-T

http://identifiers.org/hco/10/GRCh38#104359372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47930905-A-C

104359372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47930905-A-G

104359446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47930977-C-G

104360105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47931289-C-T

104360179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47931363-C-T

104361421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47931806-G-A

104361938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47932411-G-T

http://identifiers.org/hco/10/GRCh38#104362055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47932561-A-C

104362055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47932561-A-G

104362082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: 47932588-G-C

104362106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47932612-G-A

104362151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47932657-G-C

104363491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47935351-A-G

http://identifiers.org/hco/10/GRCh38#104363614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47935433-A-C

104363668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47935488-C-G

104363779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47935599-T-C

104363810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47935631-C-T

104363819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47935640-A-T

http://identifiers.org/hco/10/GRCh38#104363889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47935696-A-C

104363898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47935705-C-T

104363952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47935760-G-T

104364040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47935848-A-T

104364322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47936129-G-T

104364527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47936372-C-T

104364572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47936418-A-G

http://identifiers.org/hco/10/GRCh38#104364615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47936446-C-A

104364620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47936451-T-G

104364736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47936558-C-T

104364769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47936591-A-G

104364769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47936591-A-T

104364848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: 47936670-A-G

104364929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47936736-A-G

104364956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47936762-T-C

104365024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47936830-G-T

104365058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47936912-C-T

104365177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47937087-G-A

104365377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47937285-T-C

104365487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47937387-A-G

http://identifiers.org/hco/10/GRCh38#104365592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47937492-C-A

104365674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47937573-T-C

http://identifiers.org/hco/10/GRCh38#104365709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47937603-C-A

104365709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47937603-C-T

104365755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47937641-T-A

104365755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47937641-T-C

104365795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47937699-T-G

http://identifiers.org/hco/10/GRCh38#104365805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47937709-A-C

104365837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47937748-T-C

104365894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47937805-G-A

104365906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47937817-A-G

104365951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: stop gained
orthologous variants: 47937862-T-A

104365951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47937862-T-C

104366258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47939404-T-A

104366265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47939415-A-G

104366546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47939644-T-C

104366780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47939842-A-G

104366791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47939853-T-C

104367618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47940682-G-A

104367681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47940744-G-A

104367729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47940769-A-G

104367922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47940922-C-T

http://identifiers.org/hco/10/GRCh38#104368184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47941186-A-C

http://identifiers.org/hco/10/GRCh38#104368314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47941330-C-A

http://identifiers.org/hco/10/GRCh38#104368324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47941337-C-A

104368324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941337-C-T

104368351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941363-G-A

104368351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941363-G-C

104368351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941363-G-T

104368357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941369-T-C

104368357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941369-T-G

104368358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941370-G-T

104368360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941372-G-A

104368360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941372-G-T

104368361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941373-T-C

104368362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941374-G-C

104368362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941374-G-T

104368373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941379-T-G

104368397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941396-T-C

http://identifiers.org/hco/10/GRCh38#104368412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47941415-A-C

104368412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941415-A-T

104368638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941646-T-C

104368683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941680-G-A

104368683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941680-G-C

104368683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941680-G-T

104368850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941841-T-G

104368982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47941969-G-A

104369262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47942244-C-G

104369318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47942365-C-T

104369554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47942593-A-T

104369825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47942848-G-A

104369912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47943045-A-T

http://identifiers.org/hco/10/GRCh38#104369994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47943209-C-A

104370167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47943376-C-G

http://identifiers.org/hco/10/GRCh38#104370241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47943455-A-C

http://identifiers.org/hco/10/GRCh38#104370703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47943544-C-A

http://identifiers.org/hco/10/GRCh38#104370775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47943621-C-A

104370775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47943621-C-G

104370832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47943671-A-G

104370845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47943683-T-G

http://identifiers.org/hco/10/GRCh38#104370954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47943791-A-C

104370975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47943812-G-A

104370975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: 47943812-G-T

104371070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47943905-C-T

http://identifiers.org/hco/10/GRCh38#104371126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47943957-C-A

104371126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47943957-C-T

http://identifiers.org/hco/10/GRCh38#104371137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47943964-C-A

104371137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47943964-C-T

104371145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47943972-A-G

104371184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47943991-G-A

104371184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47943991-G-T

104371264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47944067-G-A

104372467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47944589-C-G

104372477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47944599-C-G

104372727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47944817-T-A

104373192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47946086-A-T

http://identifiers.org/hco/10/GRCh38#104376772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47946521-C-A

http://identifiers.org/hco/10/GRCh38#104376961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47946713-C-A

104377018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47946773-A-G

104377026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47946781-A-G

104377043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47946798-T-C

104377112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47946870-T-C

104377124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47946882-A-T

104377125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47946883-T-C

104377333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47947194-C-G

104377443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47947320-A-T

http://identifiers.org/hco/10/GRCh38#104377657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47947465-C-A

104377657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47947465-C-T

104377692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47947492-G-A

104378393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47948208-C-T

104378408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47948223-T-C

http://identifiers.org/hco/10/GRCh38#104378554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47948365-C-A

104378791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47948698-G-A

104378836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47948745-T-C

104378841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47948750-T-A

104379599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47950390-C-T

104379860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47950604-G-A

104379894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47950638-G-A

104379894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47950638-G-C

104379897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47950641-G-T

http://identifiers.org/hco/10/GRCh38#104379918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47950669-C-A

104379945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47950696-G-T

104380001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47950784-T-C

104380007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47950790-T-C

104380043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47950828-G-A

104380043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47950828-G-C

104380079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47950864-G-A

104380079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: 47950864-G-C

104380079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: 47950864-G-T

104380195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: 47950980-A-G

http://identifiers.org/hco/10/GRCh38#104380271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47951048-C-A

104380271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951048-C-G

104380271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951048-C-T

104380295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951080-T-A

104380322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951106-G-A

104380327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951111-T-C

104380327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951111-T-G

104380345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951129-G-A

104380345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951129-G-T

104380386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951147-G-C

104380432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951188-C-T

104380464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951219-A-G

104380494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951249-A-T

104380497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951252-C-T

104380517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951265-G-A

104380526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951271-G-A

104380526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951271-G-C

104380553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951297-A-G

104381194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47951872-A-G

104381501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47954473-C-G

104381547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47954521-C-T

104381814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47954775-T-C

104381981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47954920-A-G

http://identifiers.org/hco/10/GRCh38#104381988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47954927-C-A

http://identifiers.org/hco/10/GRCh38#104382034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47954969-A-C

104382034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47954969-A-G

http://identifiers.org/hco/10/GRCh38#104382041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47954980-C-A

104382041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47954980-C-T

104382247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47955154-C-T

104382274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47955164-G-A

104382274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47955164-G-C

104382274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47955164-G-T

http://identifiers.org/hco/10/GRCh38#104382284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47955174-C-A

104382319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47955208-C-T

104382322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47955211-T-G

104382453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47955337-T-G

104383621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47955677-C-T

104383904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47955848-A-T

104384011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47955951-T-A

104384055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47955995-C-T

104384148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47956084-C-T

104384159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47956095-T-C

104388540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47957240-G-A

104388570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47957270-G-A

104388700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47957401-C-T

104388735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47957436-T-C

104388750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47957451-G-A

104388840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47957543-A-G

104388852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47957555-G-C

104388888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47957593-T-G

104388955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47957659-T-C

104388988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47957692-G-A

104388988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47957692-G-T

104389075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47957784-C-G

104389137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47957848-T-G

104389373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47958089-A-T

104389508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47958227-G-C

104389524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47958243-G-A

104389884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47960590-G-A

104389893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47960599-T-G

104389912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47960620-T-C

104390148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47960858-T-C

104390218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47960925-A-G

104390261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47960972-T-C

104390429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47961139-C-T

104390460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47961169-A-G

104390464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47961173-A-G

104390500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47961213-C-T

http://identifiers.org/hco/10/GRCh38#104390532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47961231-C-A

104390701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47961403-G-C

104390765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47961484-A-G

104390822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47961576-T-C

104390900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47961633-G-A

104390900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47961633-G-C

104391651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: 47962407-G-T

104391694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: 47962449-A-G

104391756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: 47962510-G-T

104391916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47962666-T-G

104392084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47962817-T-G

104392155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47962880-T-C

104392209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47962934-T-A

104392209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47962934-T-C

104392539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47963260-T-C

104392612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47963332-T-C

104393171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47963753-G-A

104393249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47963815-G-C

104393249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47963815-G-T

104393268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47963834-A-G

104393376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: 47963948-G-C

104393491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47964061-T-C

http://identifiers.org/hco/10/GRCh38#104393529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47964099-C-A

104393529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47964099-C-T

104393597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47964168-G-T

104393599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47964171-T-C

104393622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47964194-A-T

104393814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47964376-A-G

104393861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47964405-C-T

104393906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47964461-T-C

104394284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47964934-A-T

104394311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47964961-C-T

104394342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47964998-A-T

104394379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47965031-T-C

104394484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47965203-T-C

104394847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47965560-G-A

104394847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47965560-G-T

104395084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47965801-G-A

104395275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47965989-G-T

104395322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47966037-A-G

104395528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47966212-G-A

104395550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47966236-A-T

104395625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47966310-T-A

104395628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47966313-C-T

104395789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47966470-A-G

104395871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47966546-A-G

104395883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47966558-T-C

http://identifiers.org/hco/10/GRCh38#104395939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47966610-C-A

104395939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47966610-C-T

104395945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47966616-A-G

104396014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47966683-A-G

104396436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47967048-G-A

104396436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47967048-G-C

104396475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47967056-A-G

104396486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47967067-T-C

104396679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47967205-G-A

104396980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47967481-T-C

104397100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47967601-T-C

104397220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47967725-T-G

http://identifiers.org/hco/10/GRCh38#104397273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47967807-C-A

104397300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47967828-T-C

104397364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47967889-G-C

104397386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47967911-G-C

104397547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47968060-G-T

104397725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47968285-C-T

http://identifiers.org/hco/10/GRCh38#104398186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47968883-C-A

104398218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47968917-T-C

104398248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47968949-C-T

104398356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47969053-A-G

104398398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47969098-C-T

104398518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47969185-A-G

104398575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47969239-T-C

104398688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47969356-C-T

104398752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47969804-C-T

104398870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47969962-C-G

104398947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970038-G-A

104399027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970105-C-G

104399040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970114-G-A

104399040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970114-G-C

104399072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970129-A-G

104399105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970162-A-G

104399105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970162-A-T

104399175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970259-A-T

104399186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970286-G-A

104399186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970286-G-T

http://identifiers.org/hco/10/GRCh38#104399217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47970317-C-A

104399217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970317-C-T

104399258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970358-G-A

104399258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970358-G-T

104399279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970379-G-A

104399279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970379-G-T

104399338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970436-T-C

104399344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970442-T-C

104399425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47970523-T-A

104399455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47970553-T-G

http://identifiers.org/hco/10/GRCh38#104399464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47970562-C-A

104399464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: 47970562-C-G

104399464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47970562-C-T

104399525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970621-G-A

104399525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970621-G-C

http://identifiers.org/hco/10/GRCh38#104399539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47970630-C-A

104399539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970630-C-T

104399617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970674-G-A

104399617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970674-G-T

104399636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970688-T-C

104399640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970692-G-A

104399640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970692-G-T

104399679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970727-A-G

104399680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970728-G-A

104399753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970877-C-T

104399834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970985-G-A

104399834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47970985-G-C

104399856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47971007-T-C

104400213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47971496-C-T

104400410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47971654-G-T

104400465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47971695-T-C

http://identifiers.org/hco/10/GRCh38#104400559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47971777-C-A

104400559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47971777-C-T

http://identifiers.org/hco/10/GRCh38#104400598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47971809-C-A

http://identifiers.org/hco/10/GRCh38#104400632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47971848-C-A

104400632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47971848-C-G

104400661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47971878-C-T

104400727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: 47971934-T-A

104400760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47971967-G-A

104400817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47972024-C-T

104400889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: 47972096-T-G

http://identifiers.org/hco/10/GRCh38#104400941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47972130-C-A

104400941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972130-C-T

104400943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972132-A-G

104400966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972154-T-A

104400966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972154-T-C

104400966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972154-T-G

104400970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972158-T-A

104400991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972180-G-A

104400991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972180-G-T

104400994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972183-G-A

104400994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972183-G-T

104400995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972184-G-A

104400995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972184-G-T

http://identifiers.org/hco/10/GRCh38#104400997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47972186-C-A

104401020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972211-A-G

104401029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972231-G-A

104401029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972231-G-T

104401032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972234-G-A

104401241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972497-T-G

104401256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972512-G-A

104401291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972547-A-G

104401395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972659-C-T

104401538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47972775-T-G

104401882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47973071-A-G

104401921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47973110-T-C

104401939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47973128-C-T

104401941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47973130-A-G

104402192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47973362-G-C

104402222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47973394-A-G

104402238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47973407-G-T

104402571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47973741-A-G

104402657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47973820-G-A

104402661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47973824-G-C

104402700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47973863-T-A

104402835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47974020-T-C

104402949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47974135-A-G

104402982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47974166-G-T

104402985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47974169-G-A

104403676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47974833-G-T

104403713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47974864-A-T

104403723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47974874-A-G

104403825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 47974976-A-G

104403825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: 47974976-A-T

http://identifiers.org/hco/10/GRCh38#104403870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47975021-C-A

104403917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47975067-A-G

104404062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47975223-A-G

104404273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47975406-C-T

104404288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47975420-C-G

104404451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47975558-T-G

104404517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47975628-G-A

104405439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47976044-A-G

104405656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47976255-C-T

104405727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47976325-A-G

104406511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47976736-G-C

104406544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47976765-T-C

104406544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47976765-T-G

http://identifiers.org/hco/10/GRCh38#104406629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47976851-A-C

104406629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47976851-A-G

104406629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47976851-A-T

104406805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47977020-G-A

104406805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47977020-G-T

104406811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47977026-T-A

104406821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47977036-G-T

http://identifiers.org/hco/10/GRCh38#104406840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47977048-C-A

http://identifiers.org/hco/10/GRCh38#104406847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47977055-C-A

104406847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47977055-C-T

104406889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47977091-G-T

104407101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47977313-A-G

104407167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47977378-A-G

104408064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47978093-G-A

104408118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47978149-G-A

104408128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47978159-C-T

104408174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47978207-G-C

104408203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47978236-G-T

104408242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47978274-G-C

http://identifiers.org/hco/10/GRCh38#104408344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47978375-C-A

104408344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47978375-C-T

104408358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47978389-T-A

104408394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47978408-G-T

104408509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47978522-T-C

104408509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47978522-T-G

104408604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47978628-G-T

104408638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47978663-A-G

104412333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47981236-T-A

104412496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47981378-T-G

104412502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47981384-T-C

http://identifiers.org/hco/10/GRCh38#104412507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47981389-C-A

104412530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47981411-G-T

http://identifiers.org/hco/10/GRCh38#104412773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47981661-C-A

104412773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47981661-C-T

104413197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47982827-C-G

104413197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47982827-C-T

104413231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47982860-T-G

104413391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47983015-G-C

http://identifiers.org/hco/10/GRCh38#104413483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47983089-C-A

104413596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47983195-C-G

104413596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47983195-C-T

104413727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47983304-T-A

104413971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47983452-C-T

104414031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47983511-A-T

104414090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47983570-C-T

104414091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47983571-G-A

104414091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47983571-G-C

104414378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47984096-C-T

104414598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47984328-G-A

104414598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47984328-G-C

104414607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47984337-G-T

http://identifiers.org/hco/10/GRCh38#104414954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47984456-C-A

104415010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47984509-G-A

104415133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47984588-A-G

104415239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47984694-G-T

104415300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47984754-G-A

104415325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47984775-A-G

104415325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47984775-A-T

104415342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47984788-A-G

104415578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47985032-C-T

104415585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47985039-G-A

104415599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47985053-T-A

104415652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47985096-C-T

104415732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47985182-A-G

104416084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47985490-C-T

104416092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47985498-A-G

104416231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47985610-C-T

104416245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47985627-G-A

104416356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47985731-G-C

104416367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47985741-C-G

104416367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47985741-C-T

104416420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47985794-T-C

104416674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47986050-A-G

104416867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47986244-C-T

104417038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47986414-G-C

104417038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47986414-G-T

104417746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47986642-A-T

104417787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47986684-A-T

104417986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47986886-T-A

http://identifiers.org/hco/10/GRCh38#104418115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47987001-C-A

104418144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47987029-G-T

104418188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47987071-C-T

104418788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47987345-A-T

104418798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47987355-G-C

104418870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47987421-T-C

104419051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47987597-G-A

104419061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47987602-T-A

http://identifiers.org/hco/10/GRCh38#104419070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47987611-C-A

104419070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47987611-C-G

104419070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47987611-C-T

104419917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47988624-A-T

104419951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47988658-A-G

104419951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47988658-A-T

104420111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47988836-T-C

104420155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47988863-G-C

104420334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47989026-A-G

104420419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47989110-T-A

104420476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47989158-T-C

104421057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47989242-C-T

104421308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47989447-C-G

104421577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47989638-T-C

104421766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47989835-G-A

104422641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47990211-C-T

104422739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47990309-G-A

104422761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47990331-T-C

104422888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47990454-C-T

104423027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47990568-G-A

104423107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47990654-T-C

104423214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47990745-G-A

http://identifiers.org/hco/10/GRCh38#104423215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47990746-C-A

104423226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47990767-A-G

104423400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47990997-G-T

104423471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47991068-T-G

http://identifiers.org/hco/10/GRCh38#104423582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47991175-C-A

104423963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47991553-T-A

104424010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47991605-C-T

104424252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47991847-C-T

104424263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47991858-C-G

104424303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47991898-G-A

104424443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47992014-C-T

104424632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47992209-G-T

104424956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47992523-C-T

104425255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47993038-T-G

104425288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47993069-G-C

104425376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47993138-G-A

104425414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47993175-A-G

104425497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47993257-A-G

104425662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47993376-T-A

104425879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47993580-G-A

104426744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47994179-G-A

104426838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47994978-T-A

104426838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47994978-T-C

104426876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47995017-T-A

104426876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47995017-T-G

http://identifiers.org/hco/10/GRCh38#104426879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47995020-C-A

104427017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47995604-A-T

104427842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47996381-T-C

104427933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47996441-C-T

http://identifiers.org/hco/10/GRCh38#104428006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47996511-C-A

104428006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47996511-C-T

104428088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47996621-A-G

104428105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47996638-A-G

104428126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47996658-G-A

104428175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47996705-G-A

104428434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47996947-G-A

104428453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47996966-T-C

104428831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47997259-G-A

http://identifiers.org/hco/10/GRCh38#104429326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47997630-A-C

104429372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47997675-A-G

104429440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47997747-G-A

104429488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47997802-T-C

104429488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47997802-T-G

104429591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47997923-C-G

104429720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47998050-C-T

http://identifiers.org/hco/10/GRCh38#104429776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#47998086-C-A

104429776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47998086-C-G

104429776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47998086-C-T

104429898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47998194-T-G

104430001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47998305-C-T

104430044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: 47998330-T-A

104430364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47998554-G-C

104430433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47998613-C-G

104431017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47999244-G-A

104431099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 47999308-G-A

104431444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48000918-T-C

104434075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48002307-A-G

104434281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48002511-G-A

104434303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48002533-G-A

104434531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48002756-A-G

104434614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48002840-G-A

104434670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48002898-C-T

104434902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48003122-C-T

104434966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48003177-A-G

104435021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48003237-A-G

http://identifiers.org/hco/10/GRCh38#104435593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48003452-A-C

104435823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48003679-G-T

104435930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48003757-C-T

104436044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48003871-A-G

104436058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48003885-C-T

104436193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004022-C-T

104436794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004191-G-A

104436885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004274-A-G

http://identifiers.org/hco/10/GRCh38#104437021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48004380-C-A

104437021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004380-C-T

104437210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004504-T-G

104437219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004512-C-T

104437231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004524-C-T

104437387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004673-T-C

104437408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004695-C-T

104437451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004744-T-A

http://identifiers.org/hco/10/GRCh38#104437479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48004776-A-C

104437676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004957-G-A

104437685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004966-T-A

104437685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004966-T-C

104437689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48004970-T-C

104437952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48005238-T-C

104438144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48005586-C-T

104440744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008005-C-T

104440794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008055-T-C

http://identifiers.org/hco/10/GRCh38#104440865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48008137-C-A

104440865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008137-C-T

104440931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008203-G-A

104441217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008248-G-A

104441288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008258-C-T

104441292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008262-C-T

104441429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008361-T-A

104441561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008500-T-C

104441682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008612-C-G

104441710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008640-T-G

104441765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008694-C-T

104441808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008735-C-T

104441960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008892-A-G

104442041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48008986-G-A

104442194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48009131-T-C

104442759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48009378-T-C

104442945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48009554-A-G

104443084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48009674-A-G

104443132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48009707-T-C

104443288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48009832-C-T

104443587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48010105-T-C

104443623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48010141-G-A

104443677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48010212-G-A

104443850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48010441-G-A

104443985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48010905-G-A

104444008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48010925-G-A

104444179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48011097-C-T

http://identifiers.org/hco/10/GRCh38#104444192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48011110-A-C

104444274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48011192-T-A

104444274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48011192-T-C

104444582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48011507-C-T

104444644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48011569-A-G

104444827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48011734-G-C

104445590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: 48012573-T-C

104445894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48012857-A-T

http://identifiers.org/hco/10/GRCh38#104445983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48012945-C-A

104446060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48013022-T-C

104446273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48013258-C-T

104446796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48013775-G-A

104446922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48013865-G-T

104447435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48014914-T-A

http://identifiers.org/hco/10/GRCh38#104447578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#48015052-C-A

104447691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 48015152-C-G

http://identifiers.org/hco/10/GRCh38#104447829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48015284-C-A

104447829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48015284-C-T

http://identifiers.org/hco/10/GRCh38#104447899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48015333-C-A

http://identifiers.org/hco/10/GRCh38#104447946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48015367-C-A

104447964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48015387-G-A

104447964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48015387-G-T

104448451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48015804-A-G

104448623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48015982-A-G

104448899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48016259-G-C

104448942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48016307-A-G

104449013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48016381-T-C

104449368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48016666-C-G

104449729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron_variant, undefined
orthologous variants: 48017113-T-C

http://identifiers.org/hco/10/GRCh38#104450003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48017438-C-A

104450145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: missense variant
orthologous variants: 48017592-T-A

104450145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: synonymous variant
orthologous variants: 48017592-T-C

104450232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48017679-T-G

104450290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48017896-G-T

104450307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48017913-T-A

104450599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48018180-C-G

104450612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48018193-A-T

104450653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48018227-T-C

104451150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48019646-G-A

104451173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48019669-T-A

104451308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48019813-G-C

104451465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48019964-A-G

104451466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48019965-C-T

http://identifiers.org/hco/10/GRCh38#104451514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48020015-A-C

104451575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48020067-T-A

104452158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48020662-T-C

104452225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48020730-T-C

104452369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48020787-G-A

http://identifiers.org/hco/10/GRCh38#104452841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48021203-C-A

104453182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48021560-G-A

http://identifiers.org/hco/10/GRCh38#104453340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48021722-C-A

104453351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48021733-A-G

104453433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48021814-A-G

104453486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48021926-C-T

104453496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48021952-C-T

104453708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48022301-C-T

http://identifiers.org/hco/10/GRCh38#104453715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48022308-A-C

104454239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48022934-G-T

http://identifiers.org/hco/10/GRCh38#104454272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48022966-C-A

104454272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48022966-C-T

http://identifiers.org/hco/10/GRCh38#104454346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48023021-C-A

104454346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: intron variant
orthologous variants: 48023021-C-T

104454590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3 prime UTR variant
orthologous variants: 48023271-G-A

104454590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3 prime UTR variant
orthologous variants: 48023271-G-C

104454590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3 prime UTR variant
orthologous variants: 48023271-G-T

http://identifiers.org/hco/10/GRCh38#104454603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48023287-A-C

104454661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3 prime UTR variant
orthologous variants: 48023357-A-G

104454739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3 prime UTR variant
orthologous variants: 48023433-T-A

104454749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3 prime UTR variant
orthologous variants: 48023443-T-C

104454816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3 prime UTR variant
orthologous variants: 48023546-C-T

http://identifiers.org/hco/10/GRCh38#104454885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#48023625-C-A

104455004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26676
most severe consequence: 3 prime UTR variant
orthologous variants: 48023746-A-G