PROK2 c.199A>C ;(p.S67R)

Variant ID: 3-71830641-T-G

NM_001126128.1(PROK2):c.199A>C;(p.S67R)

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:

Exome sequencing in 51 early onset non-familial CRC cases.

Molecular Genetics & Genomic Medicine
Thutkawkorapin, Jessada J; Lindblom, Annika A; Tham, Emma E
Publication Date: 2019-05

Variant appearance in text: PROK2: S67R
PubMed Link: 30809968
Variant Present in the following documents:
  • MGG3-7-e605-s002.xlsx, sheet 1
View BVdb publication page