ClinVar Miner

Submissions for variant NM_001982.4(ERBB3):c.890A>T (p.Asp297Val)

dbSNP: rs1057519892
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000434468 SCV000506126 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000442973 SCV000506127 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427382 SCV000506128 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000435426 SCV000506129 likely pathogenic Breast neoplasm 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000441987 SCV000506130 likely pathogenic Uterine carcinosarcoma 2016-05-31 no assertion criteria provided literature only

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