C2 c.1414G>A ;(p.A472T)

Variant ID: 6-31911055-G-A

NM_000063.4(C2):c.1414G>A;(p.A472T)

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:

Genetic testing of complement and coagulation pathways in patients with severe hypertension and renal microangiopathy.

Modern Pathology : An Official Journal Of The United States And Canadian Academy Of Pathology, Inc
Larsen, Christopher P CP; Wilson, Jon D JD; Best-Rocha, Alejandro A; Beggs, Marjorie L ML; Hennigar, Randolph A RA
Publication Date: 2018-03

Variant appearance in text: rs142243595
PubMed Link: 29148534
Variant Present in the following documents:
  • Main text
  • modpathol2017154a.pdf
View BVdb publication page