Variant #0001038751 (NC_000011.9:g.71260047G>T, NM_005553.3:c.344G>T (KRTAP5-9))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.71260047G>T
DNA change (hg38) -
Published as KRTAP5-9(NM_005553.4):c.344G>T (p.(Cys115Phe))
ISCN -
DB-ID KRTAP5-9_000001
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) 0.00377 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
KRTAP5-9 NM_005553.3 -?/. - c.344G>T r.(?) p.(Cys115Phe)


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