ClinVar Miner

Submissions for variant NM_002524.5(NRAS):c.37G>C (p.Gly13Arg)

dbSNP: rs121434595
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Total submissions: 14
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV001781267 SCV002020161 likely pathogenic Noonan syndrome 6 2019-07-08 criteria provided, single submitter clinical testing
OMIM RCV000014913 SCV000035169 pathogenic Carcinoma of colon 2009-01-01 no assertion criteria provided literature only
OMIM RCV000114743 SCV000148626 pathogenic Large congenital melanocytic nevus 2009-01-01 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000424942 SCV000503691 pathogenic Melanoma 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000434327 SCV000503692 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000444449 SCV000503693 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427817 SCV000503694 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438070 SCV000503695 likely pathogenic Acute myeloid leukemia 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419545 SCV000503696 likely pathogenic Medulloblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000426328 SCV000503697 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000437450 SCV000503698 likely pathogenic Non-Hodgkin lymphoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419583 SCV000503699 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000428963 SCV000503700 likely pathogenic Myelodysplastic syndrome 2016-05-31 no assertion criteria provided literature only
Sung Lab, Department of Medicine, Roswell Park Comprehensive Cancer Center RCV000438070 SCV003932625 pathogenic Acute myeloid leukemia 2023-06-08 no assertion criteria provided clinical testing

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