Variant #0000000997 (NC_000020.10:g.4680378A>G, PRNP(NM_000311.3):c.512A>G)

Individual ID 00000997
Chromosome 20
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.4680378A>G
Reference Appleby BS1, Appleby KK, Hall RC, Wallin MT.(2010)
DB-ID PRNP_000012
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00361 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




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.512A>G r.(?) p.(Asn171Ser) 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     
0000000997 ? ? PRNP 1 Y Yang