CFTR c.226T>G ;(p.C76G)

Variant ID: 7-117149149-T-G

NM_000492.3(CFTR):c.226T>G;(p.C76G)

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:

Frequency of CFTR, SPINK1, and cathepsin B gene mutation in North Indian population: connections between genetics and clinical data.

Thescientificworldjournal
Singh, Shweta S; Choudhuri, Gourdas G; Agarwal, Sarita S
Publication Date: 2014

Variant appearance in text: CFTR: C76G
PubMed Link: 24616641
Variant Present in the following documents:
  • Main text
  • TSWJ2014-763195.pdf
View BVdb publication page