SMARCA4 c.3150del ;(p.Y1050*)

Variant ID: 19-11136166-AC-A

NM_003072.3(SMARCA4):c.3150del;(p.Y1050*)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Germline mutations of SMARCA4 in small cell carcinoma of the ovary, hypercalcemic type and in SMARCA4-deficient undifferentiated uterine sarcoma: Clinical features of a single family and comparison of large cohorts.

Gynecologic Oncology
Connor, Yamicia D YD; Miao, Diana D; Lin, Douglas I DI; Hayne, Cynthia C; Howitt, Brooke E BE; Dalrymple, John L JL; DeLeonardis, Kimberly R KR; Hacker, Michele R MR; Esselen, Katharine M KM; Shea, Meghan M
Publication Date: 2020-04

Variant appearance in text: SMARCA4: Tyr1050fs*56
PubMed Link: 31954538
Variant Present in the following documents:
  • Main text
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SMARCA4 inactivating mutations cause concomitant Coffin-Siris syndrome, microphthalmia and small-cell carcinoma of the ovary hypercalcaemic type.

The Journal Of Pathology
Errichiello, Edoardo E; Mustafa, Noor N; Vetro, Annalisa A; Notarangelo, Lucia Dora LD; de Jonge, Hugo H; Rinaldi, Berardo B; Vergani, Debora D; Giglio, Sabrina Rita SR; Morbini, Patrizia P; Zuffardi, Orsetta O
Publication Date: 2017-09

Variant appearance in text: SMARCA4: 3150_3150delC; Tyr1050*
PubMed Link: 28608987
Variant Present in the following documents:
View BVdb publication page