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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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