ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.436G>A (p.Ala146Thr) (rs104894231)

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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000013441 SCV000033688 pathogenic Costello syndrome 2007-03-01 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438623 SCV000506622 likely pathogenic Neoplasm of uterine cervix 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000420974 SCV000506623 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432069 SCV000506624 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000444836 SCV000506625 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427320 SCV000506626 likely pathogenic Adenocarcinoma of stomach 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000434059 SCV000506627 likely pathogenic Acute myeloid leukemia 2016-05-31 no assertion criteria provided literature only

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