Variant #0000002676 (NC_000011.9:g.6636673C>G, TPP1(NM_000391.3):c.1266G>C)

Individual ID 00002676
Chromosome 11
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.6636673C>G
Reference Sleat et al. 1999 Am J Hum Genet 64:1511-1523;Steinfeld et al. 2002 Am J Med Genet 112:347-354;Taschner pers comm
DB-ID TPP1_000050
Frequency -
Average frequency (gnomAD v.2.1.1) 2.0E-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 ./. 10 c.1266G>C r.(?) p.(Gln422His) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002676 ? ? TPP1 1 Y Yang