HDAC8 c.175C>T ;(p.P59S)

Variant ID: X-71788724-G-A

NM_018486.2(HDAC8):c.175C>T;(p.P59S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: HDAC8: P59S
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page