http://identifiers.org/hco/14/GRCh38#96039368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105420169-C-A

96039368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 5 prime UTR variant
orthologous variants: 105420169-C-G

96039368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 5 prime UTR variant
orthologous variants: 105420169-C-T

96039389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 5 prime UTR variant
orthologous variants: 105420190-G-A

96039389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 5 prime UTR variant
orthologous variants: 105420190-G-C

96039389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 5 prime UTR variant
orthologous variants: 105420190-G-T

96039411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 5 prime UTR variant
orthologous variants: 105420238-G-A

96039411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 5 prime UTR variant
orthologous variants: 105420238-G-C

96039411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 5 prime UTR variant
orthologous variants: 105420238-G-T

96039457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 5 prime UTR variant
orthologous variants: 105420300-G-A

96039457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 5 prime UTR variant
orthologous variants: 105420300-G-C

96039589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, undefined
orthologous variants: 105420466-G-A

96039589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, undefined
orthologous variants: 105420466-G-T

96039618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105420487-T-A

96039685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105420550-G-A

96039685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105420550-G-T

96039729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105420586-G-C

96039752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105420614-A-T

96039948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, undefined
orthologous variants: 105420771-G-T

96040291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, missense_variant
orthologous variants: 105421080-G-T

http://identifiers.org/hco/14/GRCh38#96040360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105421148-C-A

96040369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 105421154-T-C

96040381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105421166-T-C

96040438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105421202-G-A

96040491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105421244-G-A

96040491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105421244-G-T

96040854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105421606-T-C

96041243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105421986-A-G

96042005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105422700-G-A

http://identifiers.org/hco/14/GRCh38#96042228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105422894-C-A

96042317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105423002-G-A

96042317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105423002-G-C

96042602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105423354-A-T

96042802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105423500-C-G

96042939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105423595-G-T

96043103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105423701-T-C

96043127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105423725-G-A

96043283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105423848-T-A

96043283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105423848-T-G

96043292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105423857-A-G

96043397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105423919-C-T

96043405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105423927-C-G

96043578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105424078-C-T

96043665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105424113-A-G

96043728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105424159-C-T

96043997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105424386-G-A

96044001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105424390-A-G

96044052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105424436-A-T

96044093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105424466-G-A

96044903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105424917-G-A

96045407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105425289-T-C

96045570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105425443-C-T

96045585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105425459-C-G

96045607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105425494-A-T

96045725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105426188-T-G

96045988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105426447-T-A

96046198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105426617-G-T

96046525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105426922-A-G

96046570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105426962-C-T

96046691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105427071-C-T

96046830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105427177-C-T

96046910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105427248-A-G

96047198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105428107-A-G

96047268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105428180-A-G

96047485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105428367-C-T

96047669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105428550-G-T

96051365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105434062-C-T

96051505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105434171-G-A

96051525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105434191-C-T

96051943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, undefined
orthologous variants: 105434550-G-C

96051956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105434565-G-T

96051965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105434574-C-T

96052105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, undefined
orthologous variants: 105434647-T-C

96052303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105434861-G-T

96052309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, undefined
orthologous variants: 105434867-T-C

96052309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, undefined
orthologous variants: 105434867-T-G

96052487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105434987-A-T

96052531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105435031-A-G

96052727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105435177-C-T

96052793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105435241-A-G

96052920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105435378-G-A

96053056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105435496-C-T

http://identifiers.org/hco/14/GRCh38#96053088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105435528-C-A

96053094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105435534-T-C

96053094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105435534-T-G

96053620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105437192-C-T

96053694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105437243-A-G

http://identifiers.org/hco/14/GRCh38#96053870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105437386-C-A

96054299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105437679-G-A

96054320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105437699-C-T

96054501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105437942-G-A

96054553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105438009-A-G

96054734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105438262-C-G

96054812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105438334-A-G

96054915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105438436-T-C

96062476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105439915-C-T

96062483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105439926-T-G

96062503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105439942-A-T

96062520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105439959-G-A

96062522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105439961-G-A

96062544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105439973-A-G

96062574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105440003-G-A

96062607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105440032-C-T

http://identifiers.org/hco/14/GRCh38#96062645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105440070-C-A

96062720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105440111-T-C

96063056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105440483-T-C

96063138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105440557-G-A

96065067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105440851-T-C

96065160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105440931-G-A

96065171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105440942-G-A

96065315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105441068-A-G

96065323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105441077-T-C

96065418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105441148-A-G

96065419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105441149-A-G

96065485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105441221-T-C

96065544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105441270-C-G

96065595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105441299-C-T

http://identifiers.org/hco/14/GRCh38#96065716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#105441408-C-A

96065716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, undefined
orthologous variants: 105441408-C-T

96066067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, undefined
orthologous variants: 105441671-G-C

96066072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, undefined
orthologous variants: 105441676-G-A

96066092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron_variant, undefined
orthologous variants: 105441693-C-G

96067029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105442531-T-C

96067146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105442633-G-T

96067161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105442647-T-A

96070052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105443609-G-A

http://identifiers.org/hco/14/GRCh38#96070296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105443842-A-C

96079594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105444459-C-G

96079594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105444459-C-T

96079696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105444550-T-G

http://identifiers.org/hco/14/GRCh38#96079844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105444695-A-C

96079888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105444721-A-G

96079964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105444796-C-T

96079966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105444798-G-A

96080188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105445162-T-G

96080330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105445262-C-T

96080416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105445346-G-C

96080481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105445416-A-G

http://identifiers.org/hco/14/GRCh38#96080549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105445517-C-A

96080549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105445517-C-T

96080585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105445544-C-T

96080619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105445573-T-C

http://identifiers.org/hco/14/GRCh38#96080668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105445599-C-A

96080901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105446274-T-A

96080912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105446284-G-T

96081148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105446560-C-T

http://identifiers.org/hco/14/GRCh38#96081177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105446589-A-C

96081198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105446602-C-G

96081198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105446602-C-T

http://identifiers.org/hco/14/GRCh38#96086464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105453823-C-A

96086464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105453823-C-T

http://identifiers.org/hco/14/GRCh38#96086470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105453829-C-A

96086470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105453829-C-T

http://identifiers.org/hco/14/GRCh38#96086497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105453851-C-A

96086497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: intron variant
orthologous variants: 105453851-C-T

96086603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: synonymous variant
orthologous variants: 105453956-G-A

96086603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: synonymous variant
orthologous variants: 105453956-G-C

96086627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: synonymous variant
orthologous variants: 105453980-G-A

96086627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: synonymous variant
orthologous variants: 105453980-G-T

96086797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454169-G-A

96086797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454169-G-T

96086958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454325-G-T

96086961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454328-G-A

96087009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454382-C-G

96087009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454382-C-T

96087025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454393-G-T

96087055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454425-G-C

96087074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454444-T-A

96087083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454453-G-A

96087083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454453-G-C

96087083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454453-G-T

96087085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454455-A-G

96087134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454506-G-A

96087134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454506-G-T

96087212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454589-G-T

96087241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454618-T-A

96087241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454618-T-C

96087294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105454670-A-G

96089167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105455801-A-G

96089173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105455807-G-A

96089173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105455807-G-T

96089220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105455862-G-A

96089380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456024-G-A

96089380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456024-G-T

http://identifiers.org/hco/14/GRCh38#96089394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105456038-C-A

96089415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456059-G-A

96089415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456059-G-T

96089526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456092-A-G

96089581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456137-C-T

96089595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456151-G-A

96089623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456159-G-T

http://identifiers.org/hco/14/GRCh38#96089714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105456223-C-A

96089715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456224-T-C

96089716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456225-G-A

96089716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456225-G-T

96089717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456226-A-G

96089775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456283-G-A

http://identifiers.org/hco/14/GRCh38#96089790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105456298-C-A

96089790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456298-C-T

96089802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456305-A-G

96089878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456394-T-C

96089885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456401-A-T

96089918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456429-G-A

96089918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456429-G-T

96089972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456476-G-A

96089972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456476-G-T

http://identifiers.org/hco/14/GRCh38#96089993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105456534-C-A

96089993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105456534-C-T

http://identifiers.org/hco/14/GRCh38#96090045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105456583-C-A

96092685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105458346-A-G

http://identifiers.org/hco/14/GRCh38#96092739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105458402-C-A

96092739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105458402-C-T

96092787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105458436-T-C

http://identifiers.org/hco/14/GRCh38#96092945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105458582-A-C

96092959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105458596-T-C

http://identifiers.org/hco/14/GRCh38#96093012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105458640-C-A

96093012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105458640-C-T

http://identifiers.org/hco/14/GRCh38#96093031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105458659-C-A

96093032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105458660-T-C

96093134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105458748-G-A

96093355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105458891-T-A

96093355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105458891-T-C

96093362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105458898-G-T

96093413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105458933-T-C

96093466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 105458978-T-C

http://identifiers.org/hco/14/GRCh38#96093557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105459064-C-A

96093803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3 prime UTR variant
orthologous variants: 105459270-G-T

96093965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20346
most severe consequence: 3 prime UTR variant
orthologous variants: 105459397-G-A