List of variants in gene NRAS studied for hematologic disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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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.176C>A (p.Ala59Asp)
NM_002524.5(NRAS):c.181C>A (p.Gln61Lys)	rs121913254
NM_002524.5(NRAS):c.182A>C (p.Gln61Pro)	rs11554290
NM_002524.5(NRAS):c.182A>G (p.Gln61Arg)	rs11554290
NM_002524.5(NRAS):c.182A>T (p.Gln61Leu)	rs11554290
NM_002524.5(NRAS):c.183A>C (p.Gln61His)	rs121913255
NM_002524.5(NRAS):c.183A>T (p.Gln61His)	rs121913255
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>C (p.Gly12Ala)	rs121913237
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
NM_002524.5(NRAS):c.38G>T (p.Gly13Val)	rs121434596

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