SI c.5279G>A ;(p.G1760D)

Variant ID: 3-164700167-C-T

NM_001041.3(SI):c.5279G>A;(p.G1760D)

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:

The genetic component of preeclampsia: A whole-exome sequencing study.

Plos One
Hansen, Anette Tarp AT; Bernth Jensen, Jens Magnus JM; Hvas, Anne-Mette AM; Christiansen, Mette M
Publication Date: 2018

Variant appearance in text: SI: 5279G>A; G1760D
PubMed Link: 29758065
Variant Present in the following documents:
  • Main text
  • pone.0197217.pdf
View BVdb publication page