Variant ID: 1-53787673-C-T

NM_004631.4(LRP8):c.244+4872G>A

This variant was identified in 1 publication




Publications:


Integrative mutation, haplotype and G × G interaction evidence connects ABGL4, LRP8 and PCSK9 genes to cardiometabolic risk.

Scientific Reports
T Guo, RX Yin, LM Yao, F Huang, L Pan, WX Lin, DZ Yang, SL Pan
Publication Date: 2016-11-17

Variant appearance in text: LRP8: 244+4872G>A; rs1288521
PubMed Link: 27853278
Variant Present in the following documents:
  • Main text
  • srep37375-s1.doc
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000306052.6 c.244+4872G>A - intron_variant - 2/18
ENST00000347547.2 c.244+4872G>A - intron_variant - 2/16
ENST00000354412.3 c.244+4872G>A - intron_variant - 2/15
ENST00000371454.2 c.244+4872G>A - intron_variant - 2/17
ENST00000465675.1 c.-585+4872G>A - intron_variant - 2/15
ENST00000480045.1 c.244+4872G>A - intron_variant,NMD_transcript_variant - 2/19
ENST00000496580.1 n.149+4872G>A - intron_variant,non_coding_transcript_variant - 2/2
NM_001018054.3 c.244+4872G>A - intron_variant - 2/17
NM_004631.5 c.244+4872G>A - intron_variant - 2/18
NM_017522.5 c.244+4872G>A - intron_variant - 2/15
NM_033300.4 c.244+4872G>A - intron_variant - 2/16