CFTR c.597T>G ;(p.H199Q)

Variant ID: 7-117175319-T-G

NM_000492.3(CFTR):c.597T>G;(p.H199Q)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25

Variant appearance in text: CFTR: H199Q
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 4
View BVdb publication page



Molecular analysis using DHPLC of cystic fibrosis: increase of the mutation detection rate among the affected population in Central Italy.

Bmc Medical Genetics
D'Apice, Maria Rosaria MR; Gambardella, Stefano S; Bengala, Mario M; Russo, Silvia S; Nardone, Anna Maria AM; Lucidi, Vincenzina V; Sangiuolo, Federica F; Novelli, Giuseppe G
Publication Date: 2004-04-14

Variant appearance in text: CFTR: H199Q
PubMed Link: 15084222
Variant Present in the following documents:
  • Main text
  • 1471-2350-5-8.pdf
View BVdb publication page