FCGRT c.396G>A ;(p.K132=)

Variant ID: 19-50017538-G-A

NM_001136019.2(FCGRT):c.396G>A;(p.K132=)

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:

Rare coding variants pinpoint genes that control human hematological traits.

Plos Genetics
Mousas, Abdou A; Ntritsos, Georgios G; Chen, Ming-Huei MH; Song, Ci C; Huffman, Jennifer E JE; Tzoulaki, Ioanna I; Elliott, Paul P; Psaty, Bruce M BM; , ; Auer, Paul L PL; Johnson, Andrew D AD; Evangelou, Evangelos E; Lettre, Guillaume G; Reiner, Alexander P AP
Publication Date: 2017-08

Variant appearance in text: rs150420714
PubMed Link: 28787443
Variant Present in the following documents:
  • Main text
  • pgen.1006925.pdf
View BVdb publication page