List of variants in gene NRAS reported as pathogenic for immune system cancer

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002524.5(NRAS):c.35G>A (p.Gly12Asp)	rs121913237	0.00001
NM_002524.5(NRAS):c.34G>A (p.Gly12Ser)	rs121913250
NM_002524.5(NRAS):c.34G>T (p.Gly12Cys)	rs121913250
NM_002524.5(NRAS):c.37G>C (p.Gly13Arg)	rs121434595
NM_002524.5(NRAS):c.38G>A (p.Gly13Asp)	rs121434596

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