KCTD7 c.*880T>A

Variant ID: 7-66105099-T-A

NM_153033.4(KCTD7):c.*880T>A

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:

Whole exome sequencing in Finnish families identifies new candidate genes for osteoarthritis.

Plos One
Skarp, Sini S; Kämäräinen, Olli-Pekka OP; Wei, Gong-Hong GH; Jakkula, Eveliina E; Kiviranta, Ilkka I; Kröger, Heikki H; Auvinen, Juha J; Lehenkari, Petri P; Ala-Kokko, Leena L; Männikkö, Minna M
Publication Date: 2018

Variant appearance in text: rs117143942
PubMed Link: 30157244
Variant Present in the following documents:
  • pone.0203313.s001.xlsx, sheet 3
View BVdb publication page