Variant ID: 12-102591435-TAC-ATG

NM_002674.2(PMCH):c.112_114delinsCAT;(p.Val38His)

This variant was identified in 1 publication




Publications:


Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits.

Nature Genetics
Publication Date: 2016-08

Variant appearance in text: MCH: Val38Met
PubMed Link: 27399967
Variant Present in the following documents:
  • NIHMS793138-supplement-1.pdf
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000329406.4 c.112_114delinsCAT p.Val38His missense_variant 1/3 -
NM_002674.4 c.112_114delinsCAT p.Val38His missense_variant 1/3 -