Variant #0000023038 (NC_000020.10:g.4680044_4680067del, PRNP(NM_000311.3):c.(178_201)[3])

Individual ID 00004180
Chromosome 20
Allele Parent #1
Affects function (as reported) Probably does not affect function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.4680044_4680067del
DNA change (hg38) -
Published as -
ISCN -
DB-ID PRNP_000000 See all 3 reported entries
Variant remarks Variant Error [EMISMATCH/0]: This transcript variant has an error. Please fix this entry and then remove this message.
Reference {PMID07783865:Reder 1995}
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
PRNP NM_000311.3 -?/? 2 c.(178_201)[3] r.(?) p.(Pro60_Gln67)[3] -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000004108 DNA PCRdig;SEQ - - PRNP 4 Johan den Dunnen