Variant #0000016673 (NC_000011.9:g.2846C>T, TMEM151A(NM_153266.4):c.469C>T)

Individual ID 00002117
Chromosome 11
Allele Maternal (confirmed)
Affects function (as reported) Effect unknown
Affects function (by curator) Probably affects function
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.2846C>T
Reference GenBank
DB-ID TMEM151A_000469
Frequency -
Variant remarks identified in a PKD family(Mov Disord. 2022;37(3):608-613)
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.469C>T r.469c>u p.H157Y



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002119 DNA SEQ TMEM151A 1 Yulan Chen