Variant #0000002657 (NC_000011.9:g.6637927C>A, TPP1(NM_000391.3):c.851G>T)

Individual ID 00002657
Chromosome 11
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.6637927C>A
Reference Zhong et al. 2000 Genetics in Medicine 2: 312-318;Ju et al. 2002 J Med Genet 39:822-825Moore et al 2008 Clin Genet. 74:213-22
DB-ID TPP1_000031
Frequency -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
TPP1 NM_000391.3 ./. 7 c.851G>T r.(?) p.(Gly284Val) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002657 ? ? TPP1 1 Y Yang