Variant #0000000993 (NC_000020.10:g.4680452G>A, PRNP(NM_000311.3):c.586G>A)

Individual ID 00000993
Chromosome 20
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.4680452G>A
Reference Peoc'h K1, Manivet P, Beaudry P, Attane F, Besson G, Hannequin D, Delasnerie-LauprĂȘtre N, Laplanche JL.(2000)
DB-ID PRNP_000008 See all 5 reported entries
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     
PRNP NM_000311.3 ./. 2 c.586G>A r.(?) p.(Glu196Lys) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000993 ? ? PRNP 1 Y Yang