Variant #0000319961 (NC_000004.11:g.6290800G>A, WFS1(NM_006005.3):c.402G>A)

Chromosome 4
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.6290800G>A
DNA change (hg38) g.6289073G>A
Published as WFS1(NM_001145853.1):c.402G>A (p.(Ala134=)), WFS1(NM_006005.3):c.402G>A (p.A134=)
ISCN -
DB-ID WFS1_000380 See all 2 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) 0.00096 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WFS1 NM_006005.3 -?/. - c.402G>A r.(?) p.(Ala134=)