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RET c.1700del ;(p.D567Afs*71)
Variant ID: 10-43608352-GA-G
NM_020975.4(
RET
):c.1700del;(p.D567Afs*71)
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: RET: 1700delA
PubMed Link:
17065424
Variant Present in the following documents:
Main text
View BVdb publication page