ERICH3 c.4387G>C ;(p.D1463H)

Variant ID: 1-75037007-C-G

NM_001002912.4(ERICH3):c.4387G>C;(p.D1463H)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Whole-exon sequencing of human myeloma cell lines shows mutations related to myeloma patients at relapse with major hits in the DNA regulation and repair pathways.

Journal Of Hematology & Oncology
Tessoulin, Benoît B; Moreau-Aubry, Agnès A; Descamps, Géraldine G; Gomez-Bougie, Patricia P; Maïga, Sophie S; Gaignard, Alban A; Chiron, David D; Ménoret, Emmanuelle E; Le Gouill, Steven S; Moreau, Philippe P; Amiot, Martine M; Pellat-Deceunynck, Catherine C
Publication Date: 2018-12-13

Variant appearance in text: C1orf173: 4387G>C; rs12131196
PubMed Link: 30545397
Variant Present in the following documents:
  • 13045_2018_679_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.

Scientific Reports
Chen, Xiaowei Sylvia XS; Reader, Rose H RH; Hoischen, Alexander A; Veltman, Joris A JA; Simpson, Nuala H NH; Francks, Clyde C; Newbury, Dianne F DF; Fisher, Simon E SE
Publication Date: 2017-04-25

Variant appearance in text: C1orf173: D1463H; rs12131196
PubMed Link: 28440294
Variant Present in the following documents:
  • srep46105-s2.xls, sheet 6
  • srep46105-s2.xls, sheet 8
View BVdb publication page



Embryonic signature distinguishes pediatric and adult rhabdoid tumors from other SMARCB1-deficient cancers.

Oncotarget
Richer, Wilfrid W; Masliah-Planchon, Julien J; Clement, Nathalie N; Jimenez, Irene I; Maillot, Laetitia L; Gentien, David D; Albaud, Benoît B; Chemlali, Walid W; Galant, Christine C; Larousserie, Frederique F; Boudou-Rouquette, Pascaline P; Leruste, Amaury A; Chauvin, Celine C; Han, Zhi Yan ZY; Coindre, Jean-Michel JM; Varlet, Pascale P; Freneaux, Paul P; Ranchère-Vince, Dominique D; Delattre, Olivier O; Bourdeaut, Franck F
Publication Date: 2017-05-23

Variant appearance in text: C1orf173: D1463H
PubMed Link: 28427232
Variant Present in the following documents:
  • oncotarget-08-34245-s004.xlsx, sheet 1
View BVdb publication page



A G613A missense in the Hutchinson's progeria lamin A/C gene causes a lone, autosomal dominant atrioventricular block.

Immunity & Ageing : I & A
Villa, Francesco F; Maciąg, Anna A; Spinelli, Chiara C CC; Ferrario, Anna A; Carrizzo, Albino A; Parisi, Attilio A; Torella, Annalaura A; Montenero, Chiara C; Condorelli, Gianluigi G; Vecchione, Carmine C; Nigro, Vincenzo V; Montenero, Annibale S AS; Puca, Annibale A AA
Publication Date: 2014

Variant appearance in text: C1orf173: D1463H; rs12131196
PubMed Link: 25469153
Variant Present in the following documents:
  • 12979_2014_19_MOESM2_ESM.xls, sheet 1
View BVdb publication page