ClinVar Miner

Submissions for variant NM_033360.4(KRAS):c.182A>C (p.Gln61Pro)

dbSNP: rs121913240
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000419507 SCV000504449 pathogenic Thyroid tumor 2014-10-02 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429766 SCV000504450 likely pathogenic Neoplasm of the large intestine 2015-07-14 no assertion criteria provided literature only

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