Variant #0000966562 (NC_000011.9:g.71238747dup, NM_001012503.1:c.401dup (KRTAP5-7))

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.71238747dup
DNA change (hg38) -
Published as KRTAP5-7(NM_001012503.2):c.401dupC (p.G135Rfs*20)
ISCN -
DB-ID KRTAP5-7_000009
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRTAP5-7 NM_001012503.1 -/. - c.401dup r.(?) p.(Gly135Argfs*20)


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