Variant #0000002630 (NC_000011.9:g.6640040G>A, TPP1(NM_000391.3):c.196C>T)

Individual ID 00002630
Chromosome 11
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.6640040G>A
Reference Sleat et al. 1999 Am J Hum Genet 64:1511-1523;Noher de HAc et al. 2005. Neuronal ceroid lipofuscinoses (Batten disease) in Latin America –an update, pp: 103-16.;A. Burkina pers comm
DB-ID TPP1_000004
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 ./. 3 c.196C>T r.(?) p.(Gln66*) 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     
0000002630 ? ? TPP1 1 Y Yang