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

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_002524.5(NRAS):c.179G>A (p.Gly60Glu)	rs267606920	0.00001
NM_002524.5(NRAS):c.35G>A (p.Gly12Asp)	rs121913237	0.00001
NM_002524.5(NRAS):c.149C>T (p.Thr50Ile)	rs267606921
NM_002524.5(NRAS):c.173C>T (p.Thr58Ile)	rs2101742052
NM_002524.5(NRAS):c.175G>A (p.Ala59Thr)	rs730880965
NM_002524.5(NRAS):c.182A>G (p.Gln61Arg)	rs11554290
NM_002524.5(NRAS):c.203G>T (p.Arg68Ile)
NM_002524.5(NRAS):c.34G>A (p.Gly12Ser)	rs121913250
NM_002524.5(NRAS):c.34G>C (p.Gly12Arg)	rs121913250
NM_002524.5(NRAS):c.34G>T (p.Gly12Cys)	rs121913250
NM_002524.5(NRAS):c.35G>T (p.Gly12Val)	rs121913237
NM_002524.5(NRAS):c.37G>C (p.Gly13Arg)	rs121434595
NM_002524.5(NRAS):c.38G>A (p.Gly13Asp)	rs121434596

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