PTEN c.1210T>G ;(p.*404Gext*8)

Variant ID: 10-89725227-T-G

NM_000314.4(PTEN):c.1210T>G;(p.*404Gext*8)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism.

The Journal Of Molecular Diagnostics : Jmd
Howell, Viive M VM; Cardinal, John W JW; Richardson, Anne-Louise AL; Gimm, Oliver O; Robinson, Bruce G BG; Marsh, Deborah J DJ
Publication Date: 2006-11

Variant appearance in text: PTEN: 1210T>G
PubMed Link: 17065424
Variant Present in the following documents:
  • Main text
View BVdb publication page