PRNP c.412A>C ;(p.I138L)

Variant ID: 20-4680278-A-C

NM_000311.3(PRNP):c.412A>C;(p.I138L)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Human prion protein sequence elements impede cross-species chronic wasting disease transmission.

The Journal Of Clinical Investigation
Kurt, Timothy D TD; Jiang, Lin L; Fernández-Borges, Natalia N; Bett, Cyrus C; Liu, Jun J; Yang, Tom T; Spraker, Terry R TR; Castilla, Joaquín J; Eisenberg, David D; Kong, Qingzhong Q; Sigurdson, Christina J CJ
Publication Date: 2015-04

Variant appearance in text: CJD: I138L
PubMed Link: 25705888
Variant Present in the following documents:
  • Main text
View BVdb publication page