Variant ID: 1-55519559-C-G

NM_174936.3(PCSK9):c.799+1095C>G

This variant was identified in 1 publication




Publications:


Differences in allele frequencies of autosomal dominant hypercholesterolemia SNPs in the Malaysian population.

Journal Of Human Genetics
L Alex, JK Chahil, SH Lye, P Bagali, LW Ler
Publication Date: 2012-06

Variant appearance in text: rs28385711
PubMed Link: 22534770
Variant Present in the following documents:
  • Supplemental file
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.799+1095C>G - intron_variant - 5/11
ENST00000490692.1 n.1620+1095C>G - intron_variant,non_coding_transcript_variant - 2/7
ENST00000543384.1 c.199+1095C>G - intron_variant - 3/9
NM_174936.4 c.799+1095C>G - intron_variant - 5/11
NR_110451.1 n.458+1095C>G - intron_variant,non_coding_transcript_variant - 3/9