Variant #0000001791 (NC_000019.9:g.40903062_40903065delGGAA, PRX(NM_181882.2):c.1194_1197delTTCC)

Individual ID 00001791
Chromosome 19
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.40903062_40903065delGGAA
Reference Kabzinska D1, Drac H, Sherman DL, Kostera-Pruszczyk A, Brophy PJ, Kochanski A, Hausmanowa-Petrusewicz I.(2006)
DB-ID PRX_000009
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
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.1194_1197delTTCC r.(?) p.(Leu400Trpfs*11) VariO:0141 DNA deletion VariO:0023 amphigoric amino acid indel



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001791 ? ? PRX 1 Y Yang