192796861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: 3 prime UTR variant
orthologous variants: 28644971-T-A

192797058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: 3 prime UTR variant
orthologous variants: 28645151-T-C

http://identifiers.org/hco/3/GRCh38#192797182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28645278-C-A

192797257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: 3 prime UTR variant
orthologous variants: 28645351-G-T

192797853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: 3 prime UTR variant
orthologous variants: 28645986-A-G

192797896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: 3 prime UTR variant
orthologous variants: 28646026-T-C

192798354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: 3 prime UTR variant
orthologous variants: 28646456-A-G

192798369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: 3 prime UTR variant
orthologous variants: 28646479-A-G

192798602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: synonymous variant
orthologous variants: 28646713-T-A

http://identifiers.org/hco/3/GRCh38#192798656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28646767-A-C

192799361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: synonymous variant
orthologous variants: 28647472-A-G

http://identifiers.org/hco/3/GRCh38#192799558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28647669-A-C

192799619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: synonymous variant
orthologous variants: 28647730-T-C

192799694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28647802-A-G

http://identifiers.org/hco/3/GRCh38#192799747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28648032-A-C

192799755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28648086-A-G

http://identifiers.org/hco/3/GRCh38#192799758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28648089-A-C

192799758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28648089-A-G

192799871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28648202-A-G

192799987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28648310-T-G

192800103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28648432-T-A

192802925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28648727-T-C

192803072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28648892-A-G

192803336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28649213-G-C

192803564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28649401-C-T

192803570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28649407-C-G

192803570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28649407-C-T

http://identifiers.org/hco/3/GRCh38#192804032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28649986-C-A

http://identifiers.org/hco/3/GRCh38#192804089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28650033-A-C

192804134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28650080-T-A

192804142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28650088-G-C

192804144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28650090-T-A

192804256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28650248-A-G

http://identifiers.org/hco/3/GRCh38#192804283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28650274-C-A

192804458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28650380-C-T

192804540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28650435-T-C

192804699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28650596-G-C

192804864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28650759-G-C

192805055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28651003-A-T

192805652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28651618-C-T

http://identifiers.org/hco/3/GRCh38#192805829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28651746-A-C

192805829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28651746-A-G

192806109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28651991-T-A

192806146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28652013-T-C

http://identifiers.org/hco/3/GRCh38#192806186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28652052-C-A

192806186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28652052-C-T

192806200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28652067-C-T

192806493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28652170-C-T

192806747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28652375-T-C

192806781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28652415-T-C

192807049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28652648-G-A

192807507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28653136-T-C

192807956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28653472-G-A

192807967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28653483-C-G

192807967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28653483-C-T

192807968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28653484-G-A

192808278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28653712-C-T

192808306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28653739-T-C

192808428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28653859-A-G

192808515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28653948-A-G

192808559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28653993-G-A

http://identifiers.org/hco/3/GRCh38#192808962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28654423-A-C

192809011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28654454-A-G

192809040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28654483-G-A

192809040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28654483-G-T

192809041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28654485-C-T

192809055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28654499-C-G

192809064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28654507-T-C

192810500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28655340-C-T

192810530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28655363-C-T

192810595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28655404-T-C

192810741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28655514-A-T

192810794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28655559-C-T

192810823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28655592-A-T

192810850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28655614-A-T

192810971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28655729-C-T

192811021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28655779-C-T

192812550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28656703-T-C

192814995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28657610-T-C

192815320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28657896-T-C

192815320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28657896-T-G

192815599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28658203-T-C

192815917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28658504-C-T

192815992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28658561-A-G

192816061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28658611-T-C

192816061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28658611-T-G

http://identifiers.org/hco/3/GRCh38#192816195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28658758-A-C

192816500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28659030-T-C

192816554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28659093-T-C

http://identifiers.org/hco/3/GRCh38#192816579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28659118-A-C

192816675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28659209-C-T

192816725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28659263-G-A

192817529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28661013-G-A

192817648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28661133-A-G

http://identifiers.org/hco/3/GRCh38#192817672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28661155-C-A

192817722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28661202-G-C

192817723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28661203-G-A

192817723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28661203-G-C

192817735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28661215-T-C

192817866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28661320-C-T

192818018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28661486-A-G

192818077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28661544-A-G

192818108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28661573-C-T

192818350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28661794-A-G

192818542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28661978-T-C

192818544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28661980-T-C

192818834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28662438-A-G

192818870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28662474-T-C

192818886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28662490-G-A

192818993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28662574-T-G

192819003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28662581-G-A

192819003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28662581-G-T

192819011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28662589-C-T

192819075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28662658-C-G

http://identifiers.org/hco/3/GRCh38#192819312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#28663106-C-A

192819312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28663106-C-T

192819369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28663137-G-C

192819371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28663139-G-T

192819382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28663150-C-G

192819477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28663226-G-A

192819477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28663226-G-T

192819500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28663249-C-G

192819500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28663249-C-T

192819506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28663266-G-A

192819562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28663351-A-G

192819776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28663570-G-A

192819838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28663633-A-T

192819898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28663697-C-G

http://identifiers.org/hco/3/GRCh38#192819909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28663708-C-A

192820050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28663822-T-C

192820116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28663879-G-C

192820234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28664942-A-G

192820235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28664943-C-T

192820236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28664944-A-G

192820270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28664981-G-A

192820379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665083-G-A

192820439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665154-G-A

192820449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665164-G-A

192820449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665164-G-C

192820471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665186-A-G

192820525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665240-G-A

http://identifiers.org/hco/3/GRCh38#192820568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28665282-C-A

192820658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665357-T-C

192820690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665388-C-T

192820696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665394-C-T

http://identifiers.org/hco/3/GRCh38#192821047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28665476-C-A

http://identifiers.org/hco/3/GRCh38#192821052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28665481-A-C

192821204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665611-T-C

192821243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665648-T-G

192821332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665745-G-A

192821426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665836-T-C

192821581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28665991-T-C

192821664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28666060-T-C

http://identifiers.org/hco/3/GRCh38#192821794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28666182-C-A

192821869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28666248-C-G

192822035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28666381-A-G

192822035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28666381-A-T

192822044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28666390-T-G

192822880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28667383-G-A

192822880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28667383-G-C

192823426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28667949-G-C

192824001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28668910-G-C

http://identifiers.org/hco/3/GRCh38#192824195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28669071-C-A

192824294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28669150-T-C

192824345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28669162-A-T

192824799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28669549-A-T

192824814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28669563-G-A

192825027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28669684-G-A

192825335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28669872-C-T

192825336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28669873-G-A

192826301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28670819-G-T

192826315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28670834-C-T

192826333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28670852-C-T

192826454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28670962-G-A

192826547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28671053-C-G

192826578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28671083-G-T

192830220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28676854-C-T

192830233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28676870-T-C

192830245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28676894-T-A

192830272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28676921-G-T

192830276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28676925-C-G

192830286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28676963-G-A

192830340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677015-T-A

192830340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677015-T-C

192830386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677074-C-G

192830527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677217-C-T

192830528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677218-C-T

192830751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677396-C-T

192830761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677405-C-T

192830762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677406-T-C

192830809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677452-C-G

192830913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677549-A-T

192831032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677667-T-C

192831098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677735-T-C

http://identifiers.org/hco/3/GRCh38#192831298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28677890-C-A

http://identifiers.org/hco/3/GRCh38#192831327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28677916-C-A

192831361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677933-C-T

192831363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28677935-C-G

192831720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28678280-T-C

192831730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28678290-G-C

192831831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28678392-T-C

192831974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28678524-C-T

192832036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28678587-G-A

192832098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28678654-T-A

192832525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28679149-G-C

http://identifiers.org/hco/3/GRCh38#192833492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#28679433-C-A

192833492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28679433-C-G

192833536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28679477-A-G

192833558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28679505-G-A

192833586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28679533-G-A

192834389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28680274-A-T

192834408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28680293-T-A

192835835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28681548-G-A

192835944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28681637-T-C

192836032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28681727-G-C

192836179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28681892-T-G

192836437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28682108-T-A

192836612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28682285-G-A

192836745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28682414-A-G

192837119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28683801-T-C

192837133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28683815-T-C

192837220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28683900-T-C

192837318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28683998-A-G

192837359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28684039-C-T

http://identifiers.org/hco/3/GRCh38#192837969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28684506-A-C

192838054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28684765-T-C

192838068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28684779-C-T

192838222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28684923-T-C

192838241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28684942-A-G

192838335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28685036-C-T

192838363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28685060-C-T

192839126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28685798-A-G

192839235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28685910-G-C

192839422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28686119-C-T

192839854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28686580-T-C

192839891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28686676-G-A

http://identifiers.org/hco/3/GRCh38#192839971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28686775-C-A

192840087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28686968-G-A

http://identifiers.org/hco/3/GRCh38#192840111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28686989-C-A

192840155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28687044-T-C

http://identifiers.org/hco/3/GRCh38#192840366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28687265-A-C

192840391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28687290-G-T

192840596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688108-C-T

192840603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688115-G-A

192840712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688218-A-G

192840884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688349-C-G

192840938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688403-T-C

192840938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688403-T-G

192840958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688416-T-C

192841139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688575-T-C

192841192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688621-G-T

192841215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688638-G-C

192841328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688743-T-C

192841421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688830-C-G

192841507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688894-A-G

http://identifiers.org/hco/3/GRCh38#192841612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28688990-C-A

192841612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28688990-C-T

192841786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28689149-C-T

192841814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28689178-C-G

192841814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28689178-C-T

192841837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28689229-G-T

192842238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28689798-G-C

192842260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28689817-T-C

http://identifiers.org/hco/3/GRCh38#192842398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28689940-A-C

192842398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28689940-A-G

192842479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28690020-T-C

192842881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28690420-G-A

192842892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28690431-G-A

192842892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28690431-G-C

192842920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28690444-T-C

192842977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28690491-T-G

192843006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28690519-C-T

http://identifiers.org/hco/3/GRCh38#192843020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28690533-C-A

192843297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28690786-G-C

192843683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28691356-C-G

192844062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28691623-T-C

192844257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28691770-T-C

http://identifiers.org/hco/3/GRCh38#192844455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28691969-C-A

192844455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28691969-C-G

192844455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28691969-C-T

192844513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28692014-T-A

192844536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28692032-C-T

192844928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28692369-T-C

192844990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28692429-G-A

192845096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28692529-T-C

192845197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28692623-G-A

192845391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28693283-T-C

192845518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28693389-C-T

192845563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28693417-C-T

192845609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28693463-T-C

192845683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28693542-T-C

192846106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28693626-T-A

192846215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28693740-A-T

192846261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28693786-C-G

192846354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28693822-A-G

192846563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28693990-C-T

192846661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28694463-T-C

192846756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28694566-A-T

192847303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28694987-A-G

192847334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28695014-T-C

192847335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28695015-A-G

192847387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28695062-C-T

192847436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28695108-A-G

192847712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28695619-C-T

192847714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28695621-G-A

192847790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28695690-A-G

192848019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28695925-C-T

192848081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28695988-G-A

192848082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28695989-G-A

192848207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28696113-G-A

192848339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28696259-A-G

192850279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28698235-G-A

192850356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28698303-T-C

192850471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28698420-C-T

192850528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28698479-C-G

192850944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28698869-A-G

192851029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28698948-A-T

192851097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28699018-G-A

192851109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28699030-A-G

192851172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28699083-A-G

192851318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28699243-G-A

192851369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28699295-T-G

192851988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28699555-T-C

192852005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28699572-T-A

192852005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28699572-T-C

192852009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28699576-T-C

192852157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28699725-A-G

192852213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28699763-C-G

192852223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28699777-T-C

192852223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28699777-T-G

192852325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28699872-C-T

192852326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28699873-G-A

192852449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28699965-C-T

192852694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28700201-C-G

192852789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28700278-T-C

192852883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28700374-G-A

192853008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28700542-G-A

192853076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28700586-T-G

192853331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28700778-C-T

192857123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28702309-G-A

192857353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28702540-T-C

192857438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28702622-G-C

192859192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28702894-A-G

192859530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28703028-T-C

http://identifiers.org/hco/3/GRCh38#192859588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28703089-C-A

192859792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28703227-G-A

192859867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28703301-A-G

192859970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28703351-T-C

192859970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28703351-T-G

192860272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28703685-C-T

http://identifiers.org/hco/3/GRCh38#192860420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28704211-C-A

192860460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28704251-A-G

192860498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28704279-T-C

http://identifiers.org/hco/3/GRCh38#192860513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28704293-A-C

192860538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28704318-A-G

192860634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28704414-G-C

192860685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28704480-G-A

192860940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28704735-G-A

http://identifiers.org/hco/3/GRCh38#192860971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28704765-A-C

http://identifiers.org/hco/3/GRCh38#192865604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28707558-A-C

192865613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28707563-G-A

192865649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28707598-T-A

192865649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28707598-T-C

192866169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28707795-A-G

192866463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28709171-T-C

192866799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28709481-T-C

192867031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28709690-G-A

192867038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28709697-C-T

192867039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28709698-G-A

192867050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28709709-G-T

192867081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28709749-T-G

192867169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28709821-G-A

192867169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28709821-G-C

192867169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28709821-G-T

192867295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28709910-T-C

http://identifiers.org/hco/3/GRCh38#192867459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28710038-A-C

192867649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28710246-T-G

192867729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28710324-G-T

192867768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28710368-G-A

192867769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28710369-G-A

192867977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28710534-C-T

192867990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28710547-G-A

192867990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28710547-G-C

192868245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28711202-A-G

192868283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28711229-A-G

192874684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28712314-T-G

192874908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28712512-C-G

192874918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28712524-T-G

192875095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28712679-G-A

192875096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28712680-T-C

192875136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28712708-T-C

192875177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28712753-A-G

192876029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28714019-C-G

192876126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28714119-T-C

192876184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28714158-A-G

192876298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28714263-G-A

192876298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28714263-G-C

192876408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28714447-T-C

http://identifiers.org/hco/3/GRCh38#192876522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28714562-A-C

192876917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28714991-C-G

192876963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28715033-C-T

192877009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28715071-C-T

192877054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28715115-A-G

192877263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28715303-G-C

192877393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28715422-T-A

192877666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28715670-C-T

192877668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28715672-T-C

192877711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28715702-T-C

192877801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28715811-A-T

192877853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28715864-G-A

192877890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28715902-G-A

http://identifiers.org/hco/3/GRCh38#192877931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28715944-C-A

192877964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28715987-T-A

192878469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28716743-G-A

192878469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28716743-G-C

192878476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28716750-T-C

http://identifiers.org/hco/3/GRCh38#192878486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28716760-C-A

192878659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28716926-G-A

192879571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28717447-G-A

http://identifiers.org/hco/3/GRCh38#192879734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28717598-A-C

192879913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28717777-G-C

192879954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28717808-C-T

http://identifiers.org/hco/3/GRCh38#192879981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28717834-C-A

192880427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28717915-C-G

192880578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28718027-G-A

192881375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28718559-G-C

192881606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28718786-C-T

192881620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28718800-T-C

192881637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28718806-A-G

192881901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28719027-T-G

192882011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28719102-G-A

192882021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28719113-T-C

192882102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28719196-T-A

192882525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28719360-C-T

192882547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28719382-A-T

192882629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28719433-G-A

http://identifiers.org/hco/3/GRCh38#192882729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28719534-A-C

192882729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28719534-A-T

192883350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28719672-T-A

192883350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28719672-T-C

192883426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28719745-A-G

192883839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28720118-C-G

192883839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28720118-C-T

192885056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28721451-A-G

192885077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28721473-T-C

192885090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28721486-G-A

192885199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28721601-A-G

192885335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28721720-C-T

192885509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28721896-C-T

192885563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28721945-A-G

192885621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28722003-G-A

192885881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28722282-G-A

192886397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28722801-T-C

192886623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28723019-C-T

192887068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28723392-G-A

192887091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28723415-G-A

192887182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28723502-T-A

192887182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28723502-T-C

http://identifiers.org/hco/3/GRCh38#192887296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28723605-C-A

192887338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28723646-T-C

192887689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28723897-A-G

192887742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28723952-T-C

192887840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28724068-C-G

192887840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28724068-C-T

192887943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28724136-G-C

192887952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28724145-T-C

192888076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28724251-C-T

192888096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28724269-C-T

192888544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28725163-G-C

192888685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28725298-C-T

192888686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28725299-G-A

192888686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28725299-G-C

192888921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28725477-G-A

192889125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28725623-T-C

192889186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28725751-G-T

192889318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28725846-G-C

192889336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28725864-G-A

192889344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28725871-C-T

192889438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28725957-G-C

192889611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28726107-T-C

http://identifiers.org/hco/3/GRCh38#192890225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28726719-A-C

192890264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28726766-A-G

192890385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28726878-T-C

192890444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28726964-G-A

192890545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28727008-G-A

http://identifiers.org/hco/3/GRCh38#192890568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28727032-C-A

192890603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28727053-C-T

192891195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28728144-C-G

192891220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28728169-T-C

192891230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28728179-T-C

192891315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28728268-C-T

192891316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28728269-G-A

192891450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28728346-T-C

192891510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28728406-A-G

192891528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28728424-G-C

192891766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28729303-T-A

192891811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28729348-G-A

192891959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28729490-T-C

192892068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28729602-T-A

192892228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28729741-T-C

192892584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28729906-G-T

192893069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28730261-G-A

192893070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28730262-A-G

192893089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28730281-A-G

192893210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28730384-G-A

192893571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28730677-G-C

192893618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28730725-T-C

192894449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28730871-T-C

http://identifiers.org/hco/3/GRCh38#192896666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28733087-C-A

192896756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28733156-G-T

192901756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28734823-T-G

192901946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28735000-A-G

192902010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28735065-A-G

192902485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28735493-A-G

192902521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28735516-G-C

192903301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28736196-T-C

192904510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28737563-G-A

192904532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28737579-T-G

192904610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28737643-T-C

192904705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28737731-C-T

192904919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28738124-A-G

http://identifiers.org/hco/3/GRCh38#192904935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28738140-C-A

192904935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28738140-C-T

192905100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28738314-A-G

http://identifiers.org/hco/3/GRCh38#192905226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28738465-A-C

192906307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28739624-A-T

192906531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28739757-C-T

192906568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28739792-C-T

http://identifiers.org/hco/3/GRCh38#192906603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28739806-A-C

192906705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28739905-T-C

192906767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28739970-T-C

192906879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28740076-C-T

192907150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28740370-A-G

192907193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28740410-T-C

192907199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28740416-C-T

192907235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28740452-G-T

http://identifiers.org/hco/3/GRCh38#192907297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#28740506-A-C

192907892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28741060-G-A

192907974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28741144-C-T

192908008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28741181-G-A

192910671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28742548-T-G

192910842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28742718-G-A

192910842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28742718-G-T

192910926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28742790-A-G

192911175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28743030-T-C

192911491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28743172-G-A

192911726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28743463-T-C

192911895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28743620-G-A

192911956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28743674-C-T

192912203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28743926-C-G

192912203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28743926-C-T

192912314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28744015-T-G

192912730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28744110-G-A

192913982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28744823-G-A

192914004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28744860-T-C

192914393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28745207-C-G

192914661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28745479-T-C

192914683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28745500-C-T

192914729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28745525-T-C

192915219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28746022-T-A

192915403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28746222-T-C

192915833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28746630-T-C

192916770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron_variant, undefined
orthologous variants: 28747462-A-T

192916779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28747471-G-A

192917406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28748009-G-A

192917446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28748052-G-A

192917539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28748113-G-A

192917539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30438
most severe consequence: intron variant
orthologous variants: 28748113-G-T