Variant #0000016676 (NC_000011.9:g.3240T>C, TMEM151A(NM_153266.4):c.863T>C)

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.3240T>C
Reference GenBank
DB-ID TMEM151A_000863
Frequency -
Variant remarks -
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 +/+ 2 c.863T>C r.863u>c p.F288S