Variant #0000543093 (NC_000011.9:g.1651228_1651229insTGTGGGGGCTGTGGCTCCGGCTGTGG, NM_001001480.2:c.158_159insTGTGGGGGCTGTGGCTCCGGCTGTGG (KRTAP5-5))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1651228_1651229insTGTGGGGGCTGTGGCTCCGGCTGTGG
DNA change (hg38) g.1629998_1629999insTGTGGGGGCTGTGGCTCCGGCTGTGG
Published as KRTAP5-5(NM_001001480.2):c.158_159insTGTGGGGGCTGTGGCTCCGGCTGTGG (p.G54Vfs*206)
ISCN -
DB-ID KRTAP5-5_000005
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) 0.02998 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRTAP5-5 NM_001001480.2 -/. - c.158_159insTGTGGGGGCTGTGGCTCCGGCTGTGG r.(?) p.(Gly54ValfsTer206)


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