Variant #0000329265 (NC_000003.11:g.13896244T>A, WNT7A(NM_004625.3):c.355A>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.13896244T>A
DNA change (hg38) g.13854747T>A
Published as WNT7A(NM_004625.3):c.355A>T (p.(Ile119Phe))
ISCN -
DB-ID WNT7A_000003
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WNT7A NM_004625.3 ?/. - c.355A>T r.(?) p.(Ile119Phe)