Variant #0000299122 (NC_000020.10:g.4680070T>C, PRNP(NM_000311.3):c.204T>C)

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.4680070T>C
DNA change (hg38) g.4699424T>C
Published as PRNP(NM_000311.4):c.204T>C (p.P68=), PRNP(NM_001271561.2):c.115T>C (p.S39P)
ISCN -
DB-ID PRNP_000058 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00076 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
PRNP NM_000311.3 -?/. - c.204T>C r.(?) p.(Pro68=) -