ABCA1 c.6401+10A>G

Variant ID: 9-107548569-T-C

NM_005502.3(ABCA1):c.6401+10A>G

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: ABCA1: 6401+10A>G
PubMed Link: 35304488
Variant Present in the following documents:
  • 41525_2022_294_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page