Variant #0001005792 (NC_000021.8:g.46067226dup, NC_000021.8(NM_144991.2):c.82+64122dup (TSPEAR))

Chromosome 21
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.46067226dup
DNA change (hg38) -
Published as KRTAP10-11(NM_198692.2):c.851dupG (p.(Leu285fs))
ISCN -
DB-ID TSPEAR_000064
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSPEAR NM_144991.2 ?/. - c.82+64122dup r.(=) p.(=)
KRTAP12-2 NM_181684.2 ?/. - c.*19137dup r.(?) p.(=)
KRTAP12-1 NM_181686.1 ?/. - c.*34522dup r.(?) p.(=)
KRTAP10-10 NM_181688.1 ?/. - c.*9136dup r.(?) p.(=)
KRTAP10-4 NM_198687.1 ?/. - c.*72385dup r.(?) p.(=)
KRTAP10-6 NM_198688.2 ?/. - c.-54861dup r.(?) p.(=)
KRTAP10-7 NM_198689.2 ?/. - c.*45577dup r.(?) p.(=)
KRTAP10-9 NM_198690.2 ?/. - c.*19259dup r.(?) p.(=)
KRTAP10-1 NM_198691.2 ?/. - c.-107193dup r.(?) p.(=)
KRTAP10-11 NM_198692.2 ?/. - c.851dup r.(?) p.(Leu285Profs*50)
KRTAP10-2 NM_198693.2 ?/. - c.-95885dup r.(?) p.(=)
KRTAP10-5 NM_198694.2 ?/. - c.-66771dup r.(?) p.(=)
KRTAP10-8 NM_198695.2 ?/. - c.*34429dup r.(?) p.(=)
KRTAP10-3 NM_198696.2 ?/. - c.-88628dup r.(?) p.(=)
KRTAP12-3 NM_198697.2 ?/. - c.-10671dup r.(?) p.(=)
KRTAP12-4 NM_198698.1 ?/. - c.*6967dup r.(?) p.(=)
KRTAP10-12 NM_198699.1 ?/. - c.-49891dup r.(?) p.(=)


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