Variant #0000002624 (NC_000001.10:g.40539783G>A, PPT1(NM_000310.3):c.871C>T)

Individual ID 00002624
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.40539783G>A
Reference Waliany et al. Hum Mutat (Online) 15: 206-207 2000
DB-ID PPT1_000049
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
PPT1 NM_000310.3 ./. 9 c.871C>T r.(?) p.(Gln291*) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0015 protein truncation



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002624 ? ? PPT1 1 Y Yang