Variant #0000329264 (NC_000003.11:g.13860463G>A, WNT7A(NM_004625.3):c.1028C>T)

Chromosome 3
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.13860463G>A
DNA change (hg38) g.13818966G>A
Published as WNT7A(NM_004625.3):c.1028C>T (p.(Thr343Met))
ISCN -
DB-ID WNT7A_000001
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) 0.00021 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WNT7A NM_004625.3 ?/. - c.1028C>T r.(?) p.(Thr343Met)