Variant #0000342871 (NC_000004.11:g.6279306C>T, WFS1(NM_006005.3):c.124C>T)

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6279306C>T
DNA change (hg38) g.6277579C>T
Published as WFS1(NM_001145853.1):c.124C>T (p.(Arg42*)), WFS1(NM_006005.3):c.124C>T (p.R42*)
ISCN -
DB-ID WFS1_000345 See all 6 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 8.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WFS1 NM_006005.3 +/. - c.124C>T r.(?) p.(Arg42Ter)