FH c.845G>T ;(p.G282V)

Variant ID: 1-241669362-C-A

NM_000143.3(FH):c.845G>T;(p.G282V)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain: Clinical and Genetic Characterization.

Cancers
Sánchez-Heras, A Beatriz AB; Castillejo, Adela A; García-Díaz, Juan D JD; Robledo, Mercedes M; Teulé, Alexandre A; Sánchez, Rosario R; Zúñiga, Ángel Á; Lastra, Enrique E; Durán, Mercedes M; Llort, Gemma G; Yagüe, Carmen C; Ramon Y Cajal, Teresa T; López San Martin, Consol C; López-Fernández, Adrià A; Balmaña, Judith J; Robles, Luis L; Mesa-Latorre, José M JM; Chirivella, Isabel I; Fonfria, María M; Perea Ibañez, Raquel R; Castillejo, M Isabel MI; Escandell, Inés I; Gomez, Luis L; Berbel, Pere P; Soto, Jose Luis JL
Publication Date: 2020-11-05

Variant appearance in text: FH: 845G>T
PubMed Link: 33167498
Variant Present in the following documents:
  • Main text
  • cancers-12-03277.pdf
View BVdb publication page



Targeted sequencing of FH-deficient uterine leiomyomas reveals biallelic inactivating somatic fumarase variants and allows characterization of missense variants.

Modern Pathology : An Official Journal Of The United States And Canadian Academy Of Pathology, Inc
Popp, Bernt B; Erber, Ramona R; Kraus, Cornelia C; Vasileiou, Georgia G; Hoyer, Juliane J; Burghaus, Stefanie S; Hartmann, Arndt A; Beckmann, Matthias W MW; Reis, André A; Agaimy, Abbas A
Publication Date: 2020-11

Variant appearance in text: FH: 845G>T; Gly282Val
PubMed Link: 32612247
Variant Present in the following documents:
  • 41379_2020_596_MOESM2_ESM.xlsx, sheet 5
  • 41379_2020_596_MOESM2_ESM.xlsx, sheet 3
View BVdb publication page



GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25

Variant appearance in text: FH: G282V
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 4
View BVdb publication page



Structural basis of fumarate hydratase deficiency.

Journal Of Inherited Metabolic Disease
Picaud, Sarah S; Kavanagh, Kathryn L KL; Yue, Wyatt W WW; Lee, Wen Hwa WH; Muller-Knapp, Susanne S; Gileadi, Opher O; Sacchettini, James J; Oppermann, Udo U
Publication Date: 2011-06

Variant appearance in text: FH: 845G>T; G282V
PubMed Link: 21445611
Variant Present in the following documents:
  • Main text
  • 10545_2011_Article_9294.pdf
View BVdb publication page



The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency.

Bmc Medical Genetics
Bayley, Jean-Pierre JP; Launonen, Virpi V; Tomlinson, Ian P M IP
Publication Date: 2008-03-25

Variant appearance in text: FH: Gly282Val
PubMed Link: 18366737
Variant Present in the following documents:
  • 1471-2350-9-20.pdf
View BVdb publication page