Variant #0001079635 (NC_000012.11:g.14943497T>G, NM_016312.2:c.1202A>C (WBP11))

Chromosome 12
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.14943497T>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr12_009434
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs781141535
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-07-07 17:21:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WBP11 NM_016312.2 -?/. - c.1202A>C r.(?) p.(Gln401Pro)


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