Variant ID: 12-102591505-AA-GC

NM_002674.2(PMCH):c.43_44delinsGC;(p.Phe15Ala)

This variant was identified in 2 publications




Publications:


Inflammation gene variants and susceptibility to albuminuria in the U.S. population: analysis in the Third National Health and Nutrition Examination Survey (NHANES III), 1991-1994.

Bmc Medical Genetics
RM Ned, A Yesupriya, G Imperatore, DT Smelser, R Moonesinghe, MH Chang, NF Dowling
Publication Date: 2010-11-05

Variant appearance in text: MCH: F15a
PubMed Link: 21054877
Variant Present in the following documents:
  • sr01_032.pdf
View BVdb publication page



Genetic variants associated with fasting blood lipids in the U.S. population: Third National Health and Nutrition Examination Survey.

Bmc Medical Genetics
MH Chang, A Yesupriya, RM Ned, PW Mueller, NF Dowling
Publication Date: 2010-04-20

Variant appearance in text: MCH: F15a
PubMed Link: 20406466
Variant Present in the following documents:
  • sr01_032.pdf
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000329406.4 c.43_44delinsGC p.Phe15Ala missense_variant 1/3 -
NM_002674.4 c.43_44delinsGC p.Phe15Ala missense_variant 1/3 -