Variant #0000001788 (NC_000019.9:g.40902114A>T, PRX(NM_181882.2):c.2145T>A)

Individual ID 00001788
Chromosome 19
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.40902114A>T
Reference Takashima H1, Boerkoel CF, De Jonghe P, Ceuterick C, Martin JJ, Voit T, Schr?der JM, Williams A, Brophy PJ, Timmerman V, Lupski JR.(2002)
DB-ID PRX_000006
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     
PRX NM_181882.2 ./. 7 c.2145T>A r.(?) p.(Cys715*) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0015 protein truncation



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001788 ? ? PRX 1 Y Yang