HP c.116T>C ;(p.I39T)

Variant ID: 16-72090456-T-C

NM_005143.3(HP):c.116T>C;(p.I39T)

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:

Mutations of human cationic trypsinogen (PRSS1) and chronic pancreatitis.

Human Mutation
Teich, Niels N; Rosendahl, Jonas J; Tóth, Miklós M; Mössner, Joachim J; Sahin-Tóth, Miklós M
Publication Date: 2006-08

Variant appearance in text: HP: 116T>C
PubMed Link: 16791840
Variant Present in the following documents:
  • Main text
View BVdb publication page