Variant ID: 1-201286678-C-T

NM_000299.3(PKP1):c.847-22C>T

This variant was identified in 1 publication




Publications:


Integrated analyses of gene expression and genetic association studies in a founder population.

Human Molecular Genetics
DA Cusanovich, M Caliskan, C Billstrand, K Michelini, C Chavarria, S De Leon, A Mitrano, N Lewellyn, JA Elias, GL Chupp, RM Lang, SJ Shah, JM Decara, Y Gilad, C Ober
Publication Date: 2016-05-15

Variant appearance in text: rs1794867
PMID: 26931462
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000263946.3 c.847-22C>T - intron_variant - 4/14
ENST00000352845.3 c.847-22C>T - intron_variant - 4/13
ENST00000367324.3 c.847-22C>T - intron_variant - 4/13
ENST00000475988.1 n.189-22C>T - intron_variant,non_coding_transcript_variant - 2/4
NM_000299.3 c.847-22C>T - intron_variant - 4/14
NM_001005337.3 c.847-22C>T - intron_variant - 4/13