Variant #0000016688 (NC_000011.9:g.3759A>C, TMEM151A(NM_153266.4):c.1382A>C)

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.3759A>C
Reference GenBank
DB-ID TMEM151A_001273
Frequency -
Variant remarks one PKD patient was detected to have compound heterozygous variants in TMEM151A (c.469C>T and c.1382A>C). And the variant c.1382A>C was inherited from his asymptomatic father ,while the variant c.469C>T was inherited from his mother, who also had PKD.(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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM151A NM_153266.4 -?/-? 2 c.1382A>C r.1382a>c p.Q461P