CYBB c.91_92delinsGT ;(p.R31V)

Variant ID: X-37641386-CG-GT

NM_000397.3(CYBB):c.91_92delinsGT;(p.R31V)

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:

Expanding preconception carrier screening for the Jewish population using high throughput microfluidics technology and next generation sequencing.

Bmc Medical Genomics
Gal, Moran M; Khermesh, Khen K; Barak, Michal M; Lin, Min M; Lahat, Hadas H; Reznik Wolf, Haike H; Lin, Michael M; Pras, Elon E; Levanon, Erez Y EY
Publication Date: 2016-05-13

Variant appearance in text: CYBB: R31V
PubMed Link: 27175728
Variant Present in the following documents:
  • 12920_2016_184_MOESM1_ESM.xls, sheet 1
View BVdb publication page