Variant #0000016680 (NC_000011.9:g.3652_3653insG, TMEM151A(NM_153266.4):c.1275_1276insG)

Chromosome 11
Allele Maternal (confirmed)
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.3652_3653insG
Reference GenBank
DB-ID TMEM151A_001271
Frequency -
Variant remarks identified in a PKD family with autosomal dominant inheritance
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Yulan Chen
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Yulan Chen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM151A NM_153266.4 +?/+? 1 c.1275_1276insG r.1275_1276insg p.P426Afs*19