Variant #0000002577 (NC_000001.10:g.40562882A>T, PPT1(NM_000310.3):c.29T>A)

Individual ID 00002577
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.40562882A>T
Reference MitcHon et al. Hum Mol Genet 7:291-297 1998;Munroe et al. J Med Genet 35:790 1998;Das et al. J Clin Invest 102:361-370 1998;P. Ray pers comm;GOS, UK pers comm
DB-ID PPT1_000003
Frequency -
Average frequency (gnomAD v.2.1.1) 8.0E-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     
PPT1 NM_000310.3 ./. 1 c.29T>A r.(?) p.(Leu10*) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0015 protein truncation



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002577 ? ? PPT1 1 Y Yang