ClinVar Miner

Submissions for variant NM_001982.4(ERBB3):c.889G>A (p.Asp297Asn)

dbSNP: rs1057519891
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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) RCV000424484 SCV000506131 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000435185 SCV000506132 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000418815 SCV000506133 likely pathogenic Uterine carcinosarcoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429499 SCV000506134 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000435793 SCV000506135 likely pathogenic Breast neoplasm 2016-05-31 no assertion criteria provided literature only

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