List of variants in gene KRAS reported as likely pathogenic for Noonan syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.101C>G (p.Pro34Arg)	rs104894366
NM_004985.5(KRAS):c.108A>G (p.Ile36Met)	rs727503109
NM_004985.5(KRAS):c.13A>G (p.Lys5Glu)	rs193929331
NM_004985.5(KRAS):c.179G>T (p.Gly60Val)	rs727503108
NM_004985.5(KRAS):c.202A>T (p.Arg68Trp)
NM_004985.5(KRAS):c.202_204del (p.Arg68del)	rs1951405809
NM_004985.5(KRAS):c.221C>T (p.Thr74Ile)	rs1951405479
NM_004985.5(KRAS):c.229G>T (p.Gly77Cys)	rs2141509652
NM_004985.5(KRAS):c.440A>T (p.Lys147Met)
NM_004985.5(KRAS):c.451-5642A>T	rs1592798693
NM_004985.5(KRAS):c.454G>T (p.Val152Phe)	rs397517041
NM_004985.5(KRAS):c.458A>G (p.Asp153Gly)	rs104894360
NM_004985.5(KRAS):c.466T>G (p.Phe156Val)	rs397517042
NM_033360.4(KRAS):c.189G>C (p.Glu63Asp)	rs1592808357
NM_033360.4(KRAS):c.194G>T (p.Ser65Ile)	rs1555194026
NM_033360.4(KRAS):c.355G>A (p.Asp119Asn)	rs730880471
NM_033360.4(KRAS):c.458A>C (p.Glu153Ala)	rs1592798693

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