Variant ID: 1-55527239-C-T

NM_174936.3(PCSK9):c.1863+10C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Pervasive occurrence of splice-site-creating mutations and their possible involvement in genetic disorders.

Npj Genomic Medicine
Sakaguchi, Narumi N; Suyama, Mikita M
Publication Date: 2022-03-18

Variant appearance in text: PCSK9: 1863+10C>T
PubMed Link: 35304488
Variant Present in the following documents:
  • 41525_2022_294_MOESM2_ESM.xlsx
View BVdb publication page