CFTR c.3905A>G ;(p.K1302R)

Variant ID: 7-117292927-A-G

NM_000492.3(CFTR):c.3905A>G;(p.K1302R)

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:

Seminal vesicle agenesis: An uncommon cause of azoospermia.

Canadian Urological Association Journal = Journal De L'Association Des Urologues Du Canada
Bouzouita, Abderrazak A; Kerkeni, Walid W; Abouda, Hassine H; Khrouf, Mohamed M; Elloumi, Hanene H; Mnif, Najla N; Messaoud, Taieb T; Zhioua, Amel A; Zhioua, Fethi F; Chebil, Mohamed M
Publication Date: 2014-03

Variant appearance in text: CFTR: K1302R
PubMed Link: 24839497
Variant Present in the following documents:
  • Main text
View BVdb publication page