http://identifiers.org/hco/6/GRCh38#147508832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9550796-C-A

http://identifiers.org/hco/6/GRCh38#147509151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9550483-A-C

147509151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: 9550483-A-G

147509187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: 9550447-G-A

147509187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: 9550447-G-T

http://identifiers.org/hco/6/GRCh38#147509188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9550446-C-A

147509188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: 9550446-C-G

147509188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: 9550446-C-T

147509190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: 9550444-G-A

147509190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: 9550444-G-T

http://identifiers.org/hco/6/GRCh38#147509233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9550401-C-A

147509233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: 9550401-C-G

147509233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: 9550401-C-T

147509250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: 9550384-G-A

147509250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: 9550384-G-T

http://identifiers.org/hco/6/GRCh38#147509273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9550361-C-A

147509273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: synonymous variant
orthologous variants: 9550361-C-G

147509273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: synonymous variant
orthologous variants: 9550361-C-T

147509379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: 9550255-T-C

147509379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: missense variant
orthologous variants: 9550255-T-G

147509396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9550238-G-A

147509396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9550238-G-T

147509415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9550219-G-A

147509415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9550219-G-C

147509444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9550193-G-A

147509444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9550193-G-C

147509444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9550193-G-T

http://identifiers.org/hco/6/GRCh38#147509455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9550182-C-A

147509455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9550182-C-G

147509455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9550182-C-T

147509641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9550016-T-C

147509901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9549744-T-C

147509944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9549692-G-A

147510516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9549132-C-G

147510516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9549132-C-T

http://identifiers.org/hco/6/GRCh38#147510519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9549129-C-A

147510698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9548975-A-G

147510717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9548945-A-G

http://identifiers.org/hco/6/GRCh38#147510736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9548926-C-A

147510821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9548857-A-G

147510882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9548800-A-G

147510934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9548753-A-G

147511403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9548237-A-G

147511442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9548197-T-G

147511519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9548071-C-T

147511661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9547922-T-C

147511809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9547788-A-G

147511864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9547733-A-G

147512603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9547286-G-C

http://identifiers.org/hco/6/GRCh38#147514715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9546569-C-A

http://identifiers.org/hco/6/GRCh38#147514810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9546473-C-A

147514820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9546463-G-A

147515140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9546166-A-G

147515168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9546138-C-T

147515226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9546102-G-T

http://identifiers.org/hco/6/GRCh38#147515230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9546098-A-C

147515230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9546098-A-G

http://identifiers.org/hco/6/GRCh38#147515231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9546097-C-A

147515231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9546097-C-G

147515233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9546095-G-T

147515387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9545958-A-G

147515439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9545906-T-A

147515443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9545902-T-G

147515707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9545633-G-T

147516065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9545287-A-G

147516191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9545181-T-G

147516215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9545156-G-A

147516217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9545154-A-G

http://identifiers.org/hco/6/GRCh38#147516383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9545006-C-A

147516420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9544970-T-C

147516420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9544970-T-G

147516491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9544900-G-C

147516672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9544712-A-G

147516804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9544577-C-T

147516922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9544472-G-A

http://identifiers.org/hco/6/GRCh38#147517036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9544345-A-C

147517046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9544336-G-A

147517070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9544312-G-A

147517135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9544307-C-G

147517135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9544307-C-T

147517597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9542455-T-C

147517816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9542247-T-C

147518168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9541914-C-T

147518174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9541908-A-G

147518225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9541857-T-C

147518374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9541723-G-A

147518538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9541668-A-G

147518773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9541465-A-G

147519174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9541060-C-T

http://identifiers.org/hco/6/GRCh38#147519442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9540786-C-A

147519442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9540786-C-T

147519466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9540762-A-G

147519477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9540760-A-T

147519800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9540397-A-T

http://identifiers.org/hco/6/GRCh38#147520152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9540004-C-A

147520152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9540004-C-T

147520547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9539651-G-A

147520586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9539605-T-C

147521049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9538876-T-C

147521123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9538762-A-G

147521448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9538456-T-C

147521647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9538290-A-G

147522074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9537483-G-C

147522100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9537456-T-C

147522205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9537351-G-A

147522621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9537194-C-T

147522711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9537105-G-A

147522830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9537019-T-C

147522929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9536952-G-A

147523084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9536816-C-G

147523092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9536808-G-A

147523113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9536788-C-G

147523464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9536429-G-A

147523908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9535995-A-G

http://identifiers.org/hco/6/GRCh38#147524637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9535141-A-C

147524637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9535141-A-T

147524683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9535095-A-G

147524762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9535062-T-C

147524788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9535042-T-C

147525001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9534832-C-T

147525576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9528980-C-T

147530250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9526759-C-G

147530280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9526740-T-C

147530287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9526733-G-A

147530453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9526530-A-G

147530666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9526316-G-T

147530722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9526262-G-C

147530732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9526258-C-T

147530765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9526223-C-T

147533573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9524545-C-T

147534153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9523687-A-T

http://identifiers.org/hco/6/GRCh38#147534346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9523488-C-A

147534346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9523488-C-T

http://identifiers.org/hco/6/GRCh38#147543087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9523401-C-A

147543348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9523163-T-C

147543348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9523163-T-G

147543350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9523161-C-T

147543782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9522745-G-A

http://identifiers.org/hco/6/GRCh38#147544298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9522113-C-A

147544394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9522022-T-C

147544573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9521855-A-T

147544620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9521810-G-A

147544623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9521807-G-T

147544836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9521591-A-G

147545206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9521212-A-G

147545206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9521212-A-T

http://identifiers.org/hco/6/GRCh38#147545778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9520627-A-C

http://identifiers.org/hco/6/GRCh38#147545885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9520388-A-C

147545885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9520388-A-G

147546122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9520158-G-A

http://identifiers.org/hco/6/GRCh38#147546528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9519960-C-A

147546529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9519959-T-A

147546529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9519959-T-C

147546582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9519923-T-A

147546582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9519923-T-C

147546692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9519806-A-T

147546749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9519750-G-A

147546796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9519703-G-C

147546881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9519625-T-C

147547060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9519447-C-T

http://identifiers.org/hco/6/GRCh38#147547447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9519073-C-A

147547447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9519073-C-T

147547606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9518929-C-T

147547644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9518898-C-T

147547684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9518862-G-A

147547791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9518747-G-A

http://identifiers.org/hco/6/GRCh38#147548123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9518351-C-A

147548175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9518300-G-A

147548177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9518298-G-C

147548352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9518130-C-T

147548480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9517993-G-A

147548745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9517671-G-A

147548745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9517671-G-C

147549060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9516924-T-C

147549070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9516914-C-T

147549242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9516736-T-C

147549242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9516736-T-G

147549403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9516567-T-A

147549457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9516513-T-A

147549521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9516451-A-G

147549647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9516327-A-T

147549696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9516283-C-T

147551490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9515262-G-A

147551737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9515033-G-A

147551737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9515033-G-T

147551775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9514995-G-A

147551794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9514976-G-A

147551854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9514913-A-T

147552014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9514782-C-T

147552130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9514668-T-C

147552473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9514326-A-G

147552715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9514116-C-G

147552715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9514116-C-T

147552800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9514046-C-T

147553036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9513810-T-C

http://identifiers.org/hco/6/GRCh38#147553095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9513777-C-A

147553157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9513739-G-C

147553230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9513670-G-T

147553485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9513478-T-C

147553650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9513340-G-A

147553781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9513210-T-C

147553900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9513120-T-C

147553903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9513117-G-A

http://identifiers.org/hco/6/GRCh38#147553945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9513072-C-A

147554314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9512896-G-A

147554319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9512891-C-T

147554343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9512887-A-G

147554566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9512756-G-A

147554698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9512710-A-T

147554833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9512582-T-C

147555104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9512325-C-G

http://identifiers.org/hco/6/GRCh38#147555180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9512234-A-C

147555276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9512145-G-A

147556973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9511535-C-G

147556973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9511535-C-T

147557111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9511395-A-G

147557169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9511329-G-A

http://identifiers.org/hco/6/GRCh38#147557350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9511117-A-C

147557350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9511117-A-G

147557363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9511102-G-T

147557418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9511055-A-G

147557451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9511029-T-C

147557522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9510955-C-T

147557545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9510932-T-G

147557616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9510864-G-C

147557626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9510854-C-T

147557667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9510814-T-C

147557785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9510731-T-C

147557997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9510525-T-A

147558060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9510473-G-A

147558103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9510431-C-T

147558235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9510306-G-A

147558330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9510200-T-C

http://identifiers.org/hco/6/GRCh38#147558414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9510132-A-C

http://identifiers.org/hco/6/GRCh38#147558575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9509985-C-A

147558575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9509985-C-T

147558663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9509914-C-T

147559285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9509348-A-G

147559444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9509191-T-C

147559449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9509186-T-A

147559788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9508927-C-G

147559971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9508754-C-G

http://identifiers.org/hco/6/GRCh38#147560435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9508227-C-A

147560508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9508316-A-G

147560536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9508344-A-G

147560584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9508384-G-T

147560663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9508462-G-C

147560782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9508583-G-T

147561637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9507213-G-T

147562487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9506433-G-A

147562487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9506433-G-T

147562522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9506406-C-T

147563071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9506177-T-A

147563300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9505943-A-G

147563585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9505596-C-T

147563806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9505377-T-C

147564278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9504907-G-A

147564278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9504907-G-C

147564303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9504882-G-C

147564303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9504882-G-T

147564331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9504854-A-G

147564341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9504844-G-A

147564403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, missense_variant
orthologous variants: 9504782-G-A

147564403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, missense_variant
orthologous variants: 9504782-G-C

147564403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, missense_variant
orthologous variants: 9504782-G-T

http://identifiers.org/hco/6/GRCh38#147564555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9504631-C-A

147564555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9504631-C-T

http://identifiers.org/hco/6/GRCh38#147564592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9504596-C-A

147564592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9504596-C-T

147564622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9504566-G-A

147564622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9504566-G-T

147564738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9504451-G-A

147564738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9504451-G-T

147564949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9504233-T-A

147564951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9504231-A-G

147564951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9504231-A-T

147564955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9504227-G-T

147565038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9504141-G-A

147565038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9504141-G-T

147565082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9504111-G-A

http://identifiers.org/hco/6/GRCh38#147565149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9504052-A-C

http://identifiers.org/hco/6/GRCh38#147565290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9503955-C-A

147565290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503955-C-T

http://identifiers.org/hco/6/GRCh38#147565297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9503948-C-A

147565297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503948-C-T

147565324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503924-G-T

147565361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503879-G-A

147565361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503879-G-T

147565362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503878-G-T

147565364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503876-T-C

http://identifiers.org/hco/6/GRCh38#147565896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9503642-A-C

147565896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503642-A-G

147565897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503641-A-G

147565937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503594-A-G

147565985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503548-A-G

147566010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503524-T-G

147566132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503413-C-G

147566132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503413-C-T

147566152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503393-A-G

147566152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503393-A-T

147566198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503347-A-G

147566354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503205-G-A

147566425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9503132-G-A

147566808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9502751-G-T

147566826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9502734-G-A

147566827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9502733-G-T

147566874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9502697-T-C

147566921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9502648-T-C

147566982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9502587-A-G

147567054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9502528-A-G

147567054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9502528-A-T

147567079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9502503-T-C

147567258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501869-G-T

147567261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501866-A-G

147567415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501723-T-C

147567435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501705-G-T

147567462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501678-A-G

http://identifiers.org/hco/6/GRCh38#147567501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9501639-C-A

147567501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501639-C-G

147567541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501603-A-G

147567556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501587-A-G

147567612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501531-A-G

147567737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501403-A-G

147567753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501387-G-A

147567753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501387-G-T

147567754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501386-C-T

147567769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501374-A-G

147567779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501365-T-C

147567808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501340-G-A

147567812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501336-C-T

147567813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501335-A-G

147567836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501309-T-C

147567855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9501290-T-A

http://identifiers.org/hco/6/GRCh38#147567938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9500891-A-C

147567938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500891-A-G

147567969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500861-T-C

http://identifiers.org/hco/6/GRCh38#147567978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9500852-C-A

147567989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500841-G-C

147567989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500841-G-T

147568080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500761-G-A

147568151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500700-G-A

147568163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500685-T-C

147568229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500614-A-G

147568246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500592-G-A

147568246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500592-G-C

http://identifiers.org/hco/6/GRCh38#147568310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9500543-C-A

147568317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500536-T-C

147568447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500292-T-G

147568462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500271-T-C

147568500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500154-A-G

http://identifiers.org/hco/6/GRCh38#147568504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9500150-C-A

147568508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500146-T-C

147568536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500113-T-C

147568628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9500017-A-G

147568671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499976-G-C

147568708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499942-T-C

http://identifiers.org/hco/6/GRCh38#147568711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9499939-C-A

147568711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499939-C-T

http://identifiers.org/hco/6/GRCh38#147568732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9499916-C-A

147568781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499873-T-A

http://identifiers.org/hco/6/GRCh38#147568879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9499780-C-A

147568891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499768-T-C

147569045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499748-G-A

147569045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499748-G-T

147569326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499638-G-T

147569354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499625-T-C

147569354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499625-T-G

147569376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499603-A-G

147569395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499584-G-T

147569517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499450-G-A

147569527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499440-G-A

147569574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499397-G-C

147569574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499397-G-T

147569710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499222-A-G

http://identifiers.org/hco/6/GRCh38#147569732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9499203-C-A

147569746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9499189-G-A

147569799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9498911-C-T

147569860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9498855-T-C

147569860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9498855-T-G

147569887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 9498828-T-C

http://identifiers.org/hco/6/GRCh38#147569942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9498763-A-C

147570079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9498633-T-C

147570080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9498632-G-A

147570115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9498597-G-A

147570118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9498594-T-G

147570288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9498444-A-G

147570306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9498427-C-T

147570328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9498411-G-A

147570369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9498372-A-G

147570372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9498369-T-C

147570550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9498195-T-C

147570576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9498177-T-C

147570941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9498024-G-C

147570991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9497975-A-G

147571115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9497870-A-G

147571381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9497619-T-C

147571583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9497422-A-G

147571770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9497237-G-A

147571825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9497181-A-G

147572047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9496934-G-T

147572185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9496801-A-G

147572244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9496742-G-A

147572344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9496650-T-A

147572349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9496645-T-C

147572747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9496395-A-G

http://identifiers.org/hco/6/GRCh38#147573011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9495764-A-C

147573077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9495699-G-A

147573637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9495565-A-G

147573742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9495499-A-T

147574700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9494862-G-C

147574743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9494807-G-C

147575636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9492820-G-A

147575750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9492718-C-T

147575957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9492510-T-C

147576460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9492278-T-C

147576538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9492201-G-A

147576656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9492098-A-G

147576783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9491965-T-A

147576860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9491887-G-C

http://identifiers.org/hco/6/GRCh38#147577737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9490813-A-C

147578055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9490494-G-A

147578066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9490483-A-G

147578755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9488704-A-G

147579071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9488414-T-C

147579351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9488152-T-G

147579353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9488150-T-A

147580099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9487623-A-G

147580255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9487506-G-A

147580290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9487474-A-G

http://identifiers.org/hco/6/GRCh38#147580309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9487456-A-C

http://identifiers.org/hco/6/GRCh38#147580329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9487444-C-A

147580541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9487227-G-C

147580583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9487184-G-A

147580586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9487181-G-A

147580617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9487154-G-T

147580689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9487103-G-A

147580689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9487103-G-T

147580727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9487060-T-G

147580783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9487003-A-G

147580788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9486997-T-G

147580813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9486973-A-G

http://identifiers.org/hco/6/GRCh38#147580857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9486924-A-C

147580862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9486919-T-G

147581093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9486614-A-G

147581113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9486597-G-A

147581125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9486585-C-T

147581174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9486532-C-T

147581426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9486306-G-A

147581434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9486298-G-A

147581434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9486298-G-T

http://identifiers.org/hco/6/GRCh38#147581519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9486206-C-A

147581519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9486206-C-G

147581534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9486191-A-G

147581726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9485992-C-T

147581752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9485967-T-A

147581779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9485948-G-T

147582273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9485573-G-A

147582277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9485569-G-A

147582513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9485435-T-C

147582704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9485261-T-G

147582737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9485232-T-G

147582840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9485123-A-G

147582978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9484981-G-C

147583089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9484868-A-G

http://identifiers.org/hco/6/GRCh38#147583128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9484829-A-C

147583128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9484829-A-T

147583335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9484620-G-A

147583379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9484576-G-A

147583467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9484479-A-T

147583567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9484381-G-T

147583615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9484334-A-G

147583674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9484282-T-G

http://identifiers.org/hco/6/GRCh38#147583728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9484226-C-A

147583728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9484226-C-T

147583815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9483610-T-C

147584110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9483372-C-T

147584645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9483008-A-G

147584946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9482710-A-G

147584977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9482679-A-T

147585196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9482515-A-G

147585356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9482368-G-A

147585396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9482323-G-T

147585450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9482270-G-A

147585470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9482260-C-T

147585484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9482246-T-A

147585484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9482246-T-C

147585521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9482211-T-C

147585706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9482023-A-T

147585835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9481895-A-G

147585868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9481852-T-A

147585868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9481852-T-G

147585940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9481799-T-A

147586088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9481648-T-C

147586542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9481203-C-T

147586590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9481010-A-G

147586615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9480971-T-C

147586615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9480971-T-G

147588051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9479581-C-T

147588205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9479357-C-T

147588220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9479349-A-G

147589291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9478994-C-T

147589507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9478813-G-T

147589559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9478762-C-T

147589660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9478677-G-A

147589886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9478452-T-C

147589917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9478421-C-T

147591640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9477708-C-T

147591925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9477430-C-T

147592225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9477208-G-A

147592227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9477206-G-A

147592745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9476641-A-G

147592837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9476508-A-G

http://identifiers.org/hco/6/GRCh38#147592843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9476502-A-C

147593013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9476385-G-C

147593086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9476310-G-A

147593386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9475891-A-G

147593389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9475888-G-A

147593554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9475727-A-T

147593734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9475549-G-A

147594364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9475244-G-T

147594480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9475131-C-T

147594494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9475120-A-T

147594551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9475063-A-G

147594599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9475026-A-G

147594615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9475000-T-C

147594715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9474828-C-G

147595034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9474576-A-G

147595079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9474532-A-G

147595082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9474529-C-G

147595082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9474529-C-T

http://identifiers.org/hco/6/GRCh38#147595298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9474326-A-C

147595298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9474326-A-G

147595339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9474316-T-C

147595370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9474288-T-C

147595372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9474286-T-C

147595407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9474255-T-C

147595941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9473947-T-C

147595995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9473894-T-C

147596110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9473790-G-A

147596237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9473640-A-G

147596395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9473484-T-G

147596604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9473313-G-A

147596782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9472471-G-A

147596822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9472432-G-A

147597020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9472256-G-T

147597119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9472127-A-G

147597127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9472119-C-T

147597268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9471980-T-G

147597420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9471201-G-A

147597469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9471152-A-G

147597598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9471028-G-C

147597601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9471025-A-G

147597802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9470670-C-T

147597991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9470517-A-G

147598046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9470451-T-C

147598046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9470451-T-G

147598052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9470445-G-C

147598058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9470439-C-T

147598507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9470238-T-G

http://identifiers.org/hco/6/GRCh38#147598547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9470205-C-A

147598631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9470130-G-A

147598698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9470066-G-A

147598698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9470066-G-T

http://identifiers.org/hco/6/GRCh38#147598728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9470036-C-A

147598728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9470036-C-T

147599017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9469784-G-A

147599043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9469752-G-A

http://identifiers.org/hco/6/GRCh38#147599074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9469721-C-A

http://identifiers.org/hco/6/GRCh38#147599443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9469373-C-A

147599443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9469373-C-T

147599449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9469364-C-G

147599449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9469364-C-T

147599487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9469326-G-A

147599664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9469168-A-G

147600020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9468822-C-G

147600020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9468822-C-T

147600120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9468708-C-G

147600120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9468708-C-T

147600121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9468707-T-C

147600195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9468652-G-T

147600749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9468004-G-A

147600773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9467979-G-A

147600809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9467943-G-A

147600843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9467909-G-A

147600843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9467909-G-C

147600882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9467869-C-G

147600888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9467863-C-T

147600971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9467741-G-A

147601026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9467693-T-C

147601369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9467358-T-G

147601526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9467036-G-A

147601526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9467036-G-C

147601883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9466714-G-C

147602051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9466549-A-G

147602578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9465902-T-C

147602852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9465501-A-G

http://identifiers.org/hco/6/GRCh38#147602959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9465416-A-C

147602959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9465416-A-G

147602980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9465395-T-A

147603061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9465327-A-G

147603094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9465294-A-T

147603179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9465226-A-G

147603179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9465226-A-T

147603330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9465070-A-T

147603339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9465061-T-C

147603376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9465031-G-A

147603585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9464817-C-T

147603606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9464793-T-C

147603708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9464691-A-G

http://identifiers.org/hco/6/GRCh38#147603790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9464593-A-C

147603790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9464593-A-G

147603886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9464472-G-A

147603933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9464365-C-G

147603933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9464365-C-T

147604253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9462519-G-T

147604255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9462517-C-T

147604370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9462400-C-T

147604387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9462382-G-A

147604709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9462056-G-A

147604721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9462044-T-C

147604959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9461819-C-T

147604966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9461812-T-G

147605524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9461613-T-C

147609051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9458914-T-C

147609305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9458678-C-T

147609327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9458652-G-A

147609353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9458626-G-A

147609353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9458626-G-T

http://identifiers.org/hco/6/GRCh38#147609388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9458591-A-C

147609508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9458482-C-T

http://identifiers.org/hco/6/GRCh38#147609896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9458317-C-A

147610010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9458220-A-G

147610046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9458189-G-A

147610079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9458159-A-G

147610079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9458159-A-T

http://identifiers.org/hco/6/GRCh38#147610105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9458133-A-C

147610105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9458133-A-T

147610397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9457862-T-C

147610405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9457854-C-T

http://identifiers.org/hco/6/GRCh38#147610406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9457853-A-C

http://identifiers.org/hco/6/GRCh38#147610452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9457809-C-A

147610470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9457793-A-G

147610514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9457761-G-C

147610573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9457705-A-G

147610751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9457553-T-C

http://identifiers.org/hco/6/GRCh38#147610838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9457470-C-A

147610838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9457470-C-T

147611701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9457038-T-G

147611709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9457030-T-C

147613475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9456832-C-G

147613647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9456634-A-G

http://identifiers.org/hco/6/GRCh38#147613901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9456386-C-A

147613901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9456386-C-T

147613940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9456340-T-A

147613940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9456340-T-C

147613970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9456307-C-T

147614109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9456207-T-C

147615753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9455307-C-T

147616026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9455055-T-G

147617228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9454150-G-A

147617228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9454150-G-T

147617641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9453714-T-C

http://identifiers.org/hco/6/GRCh38#147617714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9453645-C-A

147617714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9453645-C-T

147617747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9453618-G-A

147618340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9453073-G-A

147618401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9453019-T-C

147618444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9452977-G-A

147618444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9452977-G-T

147618537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9452903-T-C

http://identifiers.org/hco/6/GRCh38#147618587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9452853-A-C

147618587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9452853-A-G

147618589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9452851-T-G

147618594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9452846-C-T

147618617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9452823-G-A

http://identifiers.org/hco/6/GRCh38#147618641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9452623-C-A

147618701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9452468-C-T

147618804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9452368-C-T

147618812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9452360-T-C

147619310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9451913-G-A

147619362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9451865-G-A

147619712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9451593-C-G

147619725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9451580-G-A

147619759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9451564-C-G

147620231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9451090-T-C

http://identifiers.org/hco/6/GRCh38#147620243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9451076-C-A

147620243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9451076-C-T

147620317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9451016-G-T

147620334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9450999-C-T

147620344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9450989-C-G

147620344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9450989-C-T

http://identifiers.org/hco/6/GRCh38#147620388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9450948-C-A

147620442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9450902-T-G

147620719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9450657-T-G

147620727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9450649-G-A

147621048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9450205-T-C

147621184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9450064-T-C

147621281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9449975-T-C

147621313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9449943-G-A

147621411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9449873-A-G

147621532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9449773-C-T

147622601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9449081-C-T

147623150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9448931-C-T

147623176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9448906-A-G

147623219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9448871-G-A

147623244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9448846-C-T

147623252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9448838-A-G

http://identifiers.org/hco/6/GRCh38#147623461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9448646-A-C

147623557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9448569-T-C

147623563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9448563-T-C

147623841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9448287-T-C

147624923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9447976-T-A

147624923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9447976-T-C

147624934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9447965-C-T

147625652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9447345-C-T

http://identifiers.org/hco/6/GRCh38#147626067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9446790-A-C

147626087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9446771-T-C

147626119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9446743-G-C

147626363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9446514-A-G

147626363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9446514-A-T

147626365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9446512-T-A

147626365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9446512-T-C

147626435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9446441-T-C

147626453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9446423-A-G

http://identifiers.org/hco/6/GRCh38#147626537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9446348-C-A

147626929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9445977-A-G

147626972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9445919-G-A

147627264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9445580-C-T

147627275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9445569-C-T

147627476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9445356-T-A

147628042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9444789-T-C

147632805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9441602-A-G

147632974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9441404-C-T

147633448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9438979-T-C

147633637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9438801-C-G

147635565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9438136-T-C

147635666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9438017-G-A

147637612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9437097-C-G

147637612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9437097-C-T

147637646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9437058-A-G

http://identifiers.org/hco/6/GRCh38#147637750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9436949-C-A

147637811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9436888-T-C

147637811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9436888-T-G

147637822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9436877-G-A

http://identifiers.org/hco/6/GRCh38#147638093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9436601-A-C

147638093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9436601-A-G

147638107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9436587-C-T

147638126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9436558-T-C

147638180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9436501-C-T

147638197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9436484-G-A

147638253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9436428-A-G

147638496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9436195-A-G

147638639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9436073-G-A

147638875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9435839-A-T

147638882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9435832-T-C

http://identifiers.org/hco/6/GRCh38#147638892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9435822-A-C

147638981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9435749-G-A

147639108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9435630-A-G

147639396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9435387-T-G

147639504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9435297-G-T

147639633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9435195-G-C

147639773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9435062-T-A

147639906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9434462-G-T

147640197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9434197-G-A

147640197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9434197-G-T

147640257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9434147-T-C

147640389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9434117-C-G

147640487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9434091-G-A

147640487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9434091-G-T

147640496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9434082-G-A

147640496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9434082-G-C

147640496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9434082-G-T

147640785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9433873-G-A

147640866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9433793-A-G

147641061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9433599-T-A

147641079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9433581-T-C

147641157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9433503-T-A

147641446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9433295-A-T

147641498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9433252-A-G

147641608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9433152-G-A

147641608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9433152-G-C

147641608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9433152-G-T

147641984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9432738-T-C

147642332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9432396-C-T

147642362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9432366-C-T

147642898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9431639-T-C

147642901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9431636-G-C

147643078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9431453-G-C

http://identifiers.org/hco/6/GRCh38#147643128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9431404-C-A

147643128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9431404-C-T

147643211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9431323-T-C

147643343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9431274-G-A

147643452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9431140-T-C

147643512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9431080-C-T

147643620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430964-G-A

147643675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430909-G-A

147643687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430897-G-C

http://identifiers.org/hco/6/GRCh38#147643702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9430882-A-C

147643704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430880-G-A

147643799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430822-G-A

147643799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430822-G-C

147643932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430744-C-T

147644114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430566-T-C

147644117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430563-A-G

147644118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430562-A-G

147644205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430474-T-C

147644759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430293-A-T

147644854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430199-C-T

147644920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430135-C-T

147645024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9430032-A-G

http://identifiers.org/hco/6/GRCh38#147645291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9429770-C-A

147645438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9429677-C-G

147645479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9429638-G-T

147645640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9429501-T-C

147645660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9429480-G-A

147647419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9427085-G-C

147647640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9426906-A-G

147647694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9426852-C-T

147647857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9426678-T-C

147647921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9426622-C-T

http://identifiers.org/hco/6/GRCh38#147647957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9426585-A-C

147647957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9426585-A-G

147647972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9426570-G-A

147647974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9426568-G-A

147648719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9426224-C-G

147648798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9426137-T-G

147649169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9425779-G-C

147649461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9425490-A-G

http://identifiers.org/hco/6/GRCh38#147650090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9425194-C-A

147650204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9425088-C-T

147650209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9425069-G-A

147650209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9425069-G-T

147650628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9424513-G-C

147650745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9424385-A-G

147650864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9424275-A-G

147650870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9424271-C-G

147651139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9424003-G-T

147651564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9423610-G-A

147651793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9423379-G-T

147651915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9423252-C-G

147652276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9422774-G-T

147652971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9422239-G-A

147653103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9422108-T-G

http://identifiers.org/hco/6/GRCh38#147653203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9422019-A-C

147653219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9422001-A-G

147653238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421982-T-G

147653277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421939-G-A

147653277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421939-G-T

147653416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421813-G-A

147653417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421812-T-C

http://identifiers.org/hco/6/GRCh38#147653432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9421797-C-A

147653437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421792-A-G

http://identifiers.org/hco/6/GRCh38#147653455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9421775-C-A

147653455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421775-C-G

147653455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421775-C-T

147653456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421774-G-A

147653456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421774-G-T

http://identifiers.org/hco/6/GRCh38#147653463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9421767-C-A

147653463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421767-C-T

147653670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421560-T-C

147653803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421437-C-T

147654060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421200-G-A

147654060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421200-G-T

147654235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9421045-T-C

http://identifiers.org/hco/6/GRCh38#147654817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9420134-A-C

147654866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9420084-C-T

147654895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9420055-C-G

147654900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9420050-T-A

147654950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419999-G-A

http://identifiers.org/hco/6/GRCh38#147654975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9419980-C-A

147654975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419980-C-T

147655215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419701-T-C

147655237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419682-A-G

http://identifiers.org/hco/6/GRCh38#147655248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9419670-A-C

147655248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419670-A-T

http://identifiers.org/hco/6/GRCh38#147655281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9419637-C-A

147655310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419610-C-G

147655310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419610-C-T

147655366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419555-T-C

147655426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419503-T-C

147655550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419383-T-C

147655606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419347-C-G

147655606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419347-C-T

147655788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419172-T-G

147655810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9419150-A-G

147655946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9418994-T-G

147655969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9418971-C-G

147656032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9418903-T-C

147656301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9418371-A-G

147656305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9418367-C-T

147656454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9418110-T-C

147656508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9418057-T-C

147656996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9417596-T-C

http://identifiers.org/hco/6/GRCh38#147657081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9417511-A-C

147657081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9417511-A-T

147657118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9417479-T-C

147657343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9415662-T-C

147657382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9415619-G-C

http://identifiers.org/hco/6/GRCh38#147657817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9415201-C-A

147657817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9415201-C-T

147658396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9414696-C-G

147658703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9414492-G-C

http://identifiers.org/hco/6/GRCh38#147658864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9414367-C-A

147658947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9413556-G-T

147659358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9413175-A-G

147659435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9413109-T-C

147659460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9413100-T-C

147659505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9413058-C-T

http://identifiers.org/hco/6/GRCh38#147659733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#9412801-A-C

147659878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9412662-A-G

147659906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9412634-C-T

147660444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron variant
orthologous variants: 9412139-C-T

147660983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9412028-C-T

http://identifiers.org/hco/6/GRCh38#147661044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9411967-A-C

147661044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9411967-A-G

147661365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9411508-T-G

147661454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9411418-G-A

147661958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9411253-C-T

147662628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9410609-A-G

147662680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9410557-A-G

147662756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9410455-T-A

http://identifiers.org/hco/6/GRCh38#147662967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9410245-A-C

147663169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9410059-G-A

147663936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9409634-A-T

147664158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9409399-T-C

147664313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9409247-G-A

147664366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9409194-A-G

147664371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9409189-C-G

147664558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9408998-T-C

147664650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9408901-C-T

http://identifiers.org/hco/6/GRCh38#147664746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9408802-A-C

147664861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9408674-A-G

http://identifiers.org/hco/6/GRCh38#147665014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9408524-A-C

147665014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9408524-A-G

147665229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9408309-T-C

147665255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9408283-A-G

147665595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9407868-G-A

147665739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9407732-A-G

147666243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9406947-T-A

147666318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9406868-A-G

147666441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9405821-C-G

147666550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9405737-A-G

http://identifiers.org/hco/6/GRCh38#147666576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9405718-C-A

147666636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9405657-A-G

147667181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9405181-A-G

147667677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9404746-A-T

147667786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9404641-C-T

http://identifiers.org/hco/6/GRCh38#147668054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9404394-A-C

147668054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9404394-A-G

http://identifiers.org/hco/6/GRCh38#147668195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9404268-C-A

147668294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9404189-T-C

147668322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9404161-T-C

147671630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9403902-T-C

147671630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9403902-T-G

147671847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9403738-A-G

147671847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9403738-A-T

147671849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9403736-A-G

147671849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9403736-A-T

http://identifiers.org/hco/6/GRCh38#147671860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9403725-C-A

147671860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9403725-C-T

147672118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9403499-T-C

147672268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9403350-A-G

147672465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9403047-A-G

147672689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9402795-A-G

147672877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9402565-A-G

147673009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9402432-A-G

147673067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9402389-T-C

147673502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9402010-C-T

http://identifiers.org/hco/6/GRCh38#147673807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9401628-A-C

147675125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9400373-A-T

147675405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9400104-A-G

147675414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9400095-A-G

147675453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9400070-C-G

147675516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9400013-G-A

147675516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9400013-G-T

147675631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9399914-T-C

147675679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9399896-A-G

147675679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9399896-A-T

147675820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9399732-G-A

147675838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9399714-A-G

147676094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9399459-C-T

http://identifiers.org/hco/6/GRCh38#147676135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9399418-C-A

147676135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9399418-C-G

147676144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9399409-G-T

147676440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9399121-A-T

147676552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9399031-C-T

147676573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9399008-G-A

147676573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9399008-G-T

147676716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9398872-A-T

147676820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9398791-G-A

147676828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9398783-G-A

147676828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9398783-G-T

http://identifiers.org/hco/6/GRCh38#147676959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9398671-A-C

147676979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9398650-G-A

147677261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9398390-C-T

147677731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9397948-A-G

147677731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9397948-A-T

147678100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9397610-C-T

147678602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9397101-T-C

147678809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9396894-T-C

http://identifiers.org/hco/6/GRCh38#147683085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9390958-C-A

147683337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9390714-G-C

147683548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9390506-C-T

147683560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9390494-A-G

147683683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9390444-T-C

http://identifiers.org/hco/6/GRCh38#147683768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9390360-C-A

147683885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9390250-T-C

147683907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9390227-T-C

http://identifiers.org/hco/6/GRCh38#147684002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9390137-C-A

http://identifiers.org/hco/6/GRCh38#147684073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9390065-A-C

147684579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9389570-G-A

147684687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9389470-C-T

147684718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9389438-C-T

147684810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9389353-T-G

147684828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9389341-T-C

http://identifiers.org/hco/6/GRCh38#147684843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9389326-A-C

http://identifiers.org/hco/6/GRCh38#147684995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9389179-C-A

147685711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9388505-C-G

147685716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9388494-C-T

147685722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9388482-T-A

147685764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9388424-T-C

http://identifiers.org/hco/6/GRCh38#147685988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9388187-C-A

147686211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9387929-T-C

147686261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9387893-G-A

http://identifiers.org/hco/6/GRCh38#147692650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9386394-C-A

147692696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9386347-T-A

147692815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9386263-T-C

147693111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9385963-G-A

147693550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9385526-G-A

147693581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9385496-G-C

147693581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9385496-G-T

http://identifiers.org/hco/6/GRCh38#147694249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9384949-C-A

147694999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9384172-A-G

147695194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9384002-A-G

147695256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9383909-C-G

147695487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9383685-A-T

http://identifiers.org/hco/6/GRCh38#147695498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9383674-C-A

147695611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9383577-C-T

147695776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9383423-G-A

147695818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9383381-C-T

147695936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9383262-A-G

147695974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9383224-G-A

147696009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9383188-T-G

147696493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9382138-A-G

147696695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9381628-C-T

147696794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9381533-A-G

http://identifiers.org/hco/6/GRCh38#147696927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9381396-A-C

147697035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9381187-C-T

147697054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9381167-A-G

147697054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9381167-A-T

147699260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9380200-C-T

147699282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9380178-T-G

147699377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9380103-G-T

147699439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9380042-T-C

147699470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9380011-G-C

147699808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9379673-C-T

147700602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9378856-T-C

147701097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9378353-G-A

147701181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9378288-C-T

147701190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9378279-G-A

http://identifiers.org/hco/6/GRCh38#147701951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9377868-C-A

http://identifiers.org/hco/6/GRCh38#147701981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9377838-C-A

147702581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9377137-G-A

147702632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9377083-C-T

147702716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9377002-C-G

147702716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9377002-C-T

http://identifiers.org/hco/6/GRCh38#147703636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9376210-C-A

147703636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9376210-C-T

147704417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9375775-A-G

147704468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9375724-T-C

147704489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9375703-G-A

147704605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9375593-T-G

147704743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9375476-G-C

147704745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9375474-G-A

147704762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9375457-A-G

147704869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9375354-A-G

http://identifiers.org/hco/6/GRCh38#147704930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9375293-C-A

147704997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9375230-G-T

http://identifiers.org/hco/6/GRCh38#147705046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9375182-A-C

147705046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9375182-A-T

147705114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9375115-C-G

147705345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9374913-C-T

http://identifiers.org/hco/6/GRCh38#147705444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9374843-A-C

http://identifiers.org/hco/6/GRCh38#147705450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9374837-C-A

147706017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9374292-A-G

147706033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9374273-C-T

147706795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9372282-A-G

http://identifiers.org/hco/6/GRCh38#147707123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9371946-C-A

147707197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9371840-C-G

147707509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9371308-C-T

147707697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9371113-G-A

147707739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9371071-C-T

147707768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9371041-A-G

147707815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9370995-A-G

147707845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9370965-T-C

147708047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9370775-G-A

147708092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9370732-T-A

147708126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9370697-T-A

147708174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9370658-G-T

147708726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9370524-A-T

147709072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9370232-A-G

147709081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9370223-A-G

http://identifiers.org/hco/6/GRCh38#147709610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9368835-C-A

http://identifiers.org/hco/6/GRCh38#147709994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9368442-A-C

147711141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9367868-T-C

147711438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9367583-C-T

147711725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9367291-T-C

147712137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9366885-C-T

147712200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9366822-C-T

147712215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9366807-A-G

147718072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9366527-G-A

147718398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9366233-G-A

147718398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9366233-G-T

147722165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9365125-A-G

147722375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9364898-C-G

147722456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9364817-T-A

147722456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9364817-T-C

147722508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9364766-A-T

147722707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9364571-T-A

147723208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9363307-A-G

147723245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9363271-G-A

147723325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9363184-G-A

http://identifiers.org/hco/6/GRCh38#147723431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9363082-C-A

147723431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9363082-C-T

http://identifiers.org/hco/6/GRCh38#147724482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9362155-C-A

http://identifiers.org/hco/6/GRCh38#147724492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9362145-A-C

147724532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9362107-A-G

147724601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9362036-T-G

147724609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9362028-T-A

147725023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9361625-A-G

147725268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9361379-T-C

147726120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9360867-T-C

147726293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9360701-A-G

147726497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9360477-T-C

147726614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9360422-G-A

147726699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9360351-A-G

147726770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9360277-T-C

147726784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9360263-C-T

147726893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9360158-T-A

147726963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9360112-C-T

147730324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9358997-A-G

147730349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9358972-G-A

147730349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9358972-G-C

147730349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9358972-G-T

http://identifiers.org/hco/6/GRCh38#147730447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9358878-C-A

147730774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9358501-C-T

147730854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9358398-C-T

147730937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9358218-A-T

147731408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9357774-C-G

147731408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9357774-C-T

147731543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9357642-C-G

http://identifiers.org/hco/6/GRCh38#147731684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9357476-C-A

http://identifiers.org/hco/6/GRCh38#147731694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9357466-C-A

147731696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9357464-C-T

147731700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9357460-C-T

147731708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9357452-T-C

147731720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9357440-T-C

147731800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9357223-T-A

http://identifiers.org/hco/6/GRCh38#147732254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9356803-C-A

147732342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9356716-A-G

147732455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9356603-G-A

147732645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9356438-T-A

147732676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9356407-T-C

147733391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9355333-G-A

147733415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9355316-G-A

147733415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9355316-G-T

147733694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9355049-A-G

147733699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9355044-T-C

http://identifiers.org/hco/6/GRCh38#147733704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9355039-C-A

http://identifiers.org/hco/6/GRCh38#147733780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9354962-C-A

147733815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9354928-A-G

147734116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9354636-G-A

147735692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9353082-A-G

http://identifiers.org/hco/6/GRCh38#147735936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9353025-C-A

147735936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9353025-C-T

147735973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9352993-A-G

147736011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9352956-G-A

147736102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9352873-G-T

147736229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9352739-C-T

147736257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9352721-G-A

147736270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9352709-T-C

147736831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9351599-C-T

147737166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9351267-T-C

http://identifiers.org/hco/6/GRCh38#147737205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9351227-C-A

147737205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9351227-C-T

147737230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9351205-T-C

http://identifiers.org/hco/6/GRCh38#147737241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9351194-C-A

147737241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9351194-C-G

147737241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9351194-C-T

http://identifiers.org/hco/6/GRCh38#147737271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9351164-C-A

147737271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9351164-C-T

147737325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 9351111-A-G

147737351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 9351085-G-T

http://identifiers.org/hco/6/GRCh38#147737369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9351067-C-A

147737369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 9351067-C-T

147737406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 9351030-G-A

147737406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 9351030-G-T

147737427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 9351009-T-A

147737427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 9351009-T-C

http://identifiers.org/hco/6/GRCh38#147737458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#9350979-C-A

147737458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9350979-C-T

147737462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9350975-G-T

147737473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9350970-T-C

147737502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9350941-G-T

147737701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9350743-G-C

147737701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9350743-G-T

147738429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9350023-C-T

147738430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21180
most severe consequence: intron_variant, undefined
orthologous variants: 9350022-G-A