ClinVar Miner

Submissions for variant NM_002524.5(NRAS):c.183A>C (p.Gln61His)

dbSNP: rs121913255
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000443672 SCV000503587 pathogenic Melanoma 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000426637 SCV000503588 pathogenic Non-small cell lung carcinoma 2014-10-02 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436751 SCV000503589 likely pathogenic Acute myeloid leukemia 2014-10-02 no assertion criteria provided literature only

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