Variant #0001056985 (NC_000021.8:g.31798184C>A, NM_181622.1:c.47G>T (KRTAP13-3))

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.31798184C>A
DNA change (hg38) -
Published as KRTAP13-3(NM_181622.2):c.47G>T (p.(Gly16Val))
ISCN -
DB-ID KRTAP13-3_000003
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRTAP13-4 NM_181600.1 ?/. - c.-4410C>A r.(?) p.(=)
KRTAP13-3 NM_181622.1 ?/. - c.47G>T r.(?) p.(Gly16Val)


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