Variant #0000002635 (NC_000011.9:g.6638857C>T, TPP1(NM_000391.3):c.380G>A)

Individual ID 00002635
Chromosome 11
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.6638857C>T
Reference Zhong et al. 2000 Genetics in Medicine 2: 312-318;Steinfeld et al. 2002 Am J Med Genet 112:347-353;P. Ray pers comm
DB-ID TPP1_000009
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     
TPP1 NM_000391.3 ./. 4 c.380G>A r.(?) p.(Arg127Gln) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002635 ? ? TPP1 1 Y Yang