Variant #0000023008 (NC_000020.10:g.4680216C>T, PRNP(NM_000311.3):c.350C>T)

Individual ID 00004166
Chromosome 20
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.4680216C>T
DNA change (hg38) g.4699570C>T
Published as -
ISCN -
DB-ID PRNP_000020 See all 2 reported entries
Variant remarks -
Reference {PMID08829666:Palmer 1996}
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
PRNP NM_000311.3 -/? 2 c.350C>T r.(?) p.(Ala117Val) -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000004094 DNA PCRdig;SEQ - - PRNP 2 Johan den Dunnen