ClinVar Miner

Submissions for variant NM_004448.4(ERBB2):c.2305G>C (p.Asp769His)

dbSNP: rs121913468
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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) RCV000445220 SCV000504583 pathogenic Breast neoplasm 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000423455 SCV000504584 likely pathogenic Carcinoma of esophagus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000433752 SCV000504585 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000444643 SCV000504586 likely pathogenic Neoplasm of uterine cervix 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000426351 SCV000504587 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only

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