ClinVar Miner

Submissions for variant NM_004448.3(ERBB2):c.2263_2264delinsCC (p.Leu755Pro) (rs121913469)

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Total submissions: 8
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000014891 SCV000035146 pathogenic Lung adenocarcinoma 2004-09-30 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000425374 SCV000506105 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000433907 SCV000506106 likely pathogenic Adenocarcinoma of stomach 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443258 SCV000506107 likely pathogenic Papillary renal cell carcinoma, sporadic 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000426475 SCV000506108 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436720 SCV000506109 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000420852 SCV000506110 likely pathogenic Breast neoplasm 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427611 SCV000506111 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only

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