Variant #0000023079 (NC_000020.10:g.4680115_4680116ins216, PRNP(NM_000311.3):c.249_250ins204_251ins228_251{246A>G}ins180_227{222G>A}ins204_251ins204_251)

Individual ID 00004204
Chromosome 20
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.4680115_4680116ins216
DNA change (hg38) -
Published as -
ISCN -
DB-ID PRNP_000009
Variant remarks 14-haplotype 1-2-2-3-2-3-3g-2-2a-2-3-2-3-4
Reference {PMID08750875:Krasemann 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
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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.249_250ins204_251ins228_251{246A>G}ins180_227{222G>A}ins204_251ins204_251 r.(?) p.(Pro60_Gln67)[13] -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000004132 DNA PCR;SEQ - - PRNP 1 Johan den Dunnen