Variant #0000347993 (NC_000002.11:g.219755011T>A, NM_025216.2:c.682T>A (WNT10A))

Chromosome 2
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.219755011T>A
DNA change (hg38) g.218890289T>A
Published as WNT10A(NM_025216.2):c.682T>A (p.F228I, p.(Phe228Ile)), WNT10A(NM_025216.3):c.682T>A (p.F228I)
ISCN -
DB-ID WNT10A_000001 See all 63 reported entries
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) 0.01389 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WNT10A NM_025216.2 +/. - c.682T>A r.(?) p.(Phe228Ile)


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