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SMAD3 c.658+3937T>G
Variant ID: 15-67466879-T-G
NM_005902.3(
SMAD3
):c.658+3937T>G
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:
MYO1E mutations and childhood familial focal segmental glomerulosclerosis.
The New England Journal Of Medicine
Mele, Caterina C; Iatropoulos, Paraskevas P; Donadelli, Roberta R; Calabria, Andrea A; Maranta, Ramona R; Cassis, Paola P; Buelli, Simona S; Tomasoni, Susanna S; Piras, Rossella R; Krendel, Mira M; Bettoni, Serena S; Morigi, Marina M; Delledonne, Massimo M; Pecoraro, Carmine C; Abbate, Isabella I; Capobianchi, Maria Rosaria MR; Hildebrandt, Friedhelm F; Otto, Edgar E; Schaefer, Franz F; Macciardi, Fabio F; Ozaltin, Fatih F; Emre, Sevinc S; Ibsirlioglu, Tulin T; Benigni, Ariela A; Remuzzi, Giuseppe G; Noris, Marina M; ,
Publication Date: 2011-07-28
Variant appearance in text: rs2278545
PubMed Link:
21756023
Variant Present in the following documents:
Main text
View BVdb publication page