Variant #0000002616 (NC_000001.10:g.40544293A>G, PPT1(NM_000310.3):c.665T>C)

Individual ID 00002616
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.40544293A>G
Reference Mazzei et al. J Neurol 249:1398-1400 2002;Simonati et al. Paediatr Neurol. 40:271-276 2009
DB-ID PPT1_000042
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 ./. 7 c.665T>C r.(?) p.(Leu222Pro) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002616 ? ? PPT1 1 Y Yang