ClinVar Miner

List of variants in gene KRAS reported as pathogenic for Noonan syndrome and Noonan-related syndrome

Included ClinVar conditions (50):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_004985.5(KRAS):c.35G>A (p.Gly12Asp) rs121913529
NM_033360.4(KRAS):c.*12A>T rs104894360
NM_033360.4(KRAS):c.*20T>A rs397517042
NM_033360.4(KRAS):c.*22C>G rs104894362
NM_033360.4(KRAS):c.*9T>G rs104894367
NM_033360.4(KRAS):c.101C>G (p.Pro34Arg) rs104894366
NM_033360.4(KRAS):c.101C>T (p.Pro34Leu) rs104894366
NM_033360.4(KRAS):c.108A>G (p.Ile36Met) rs727503109
NM_033360.4(KRAS):c.13A>G (p.Lys5Glu) rs193929331
NM_033360.4(KRAS):c.15A>T (p.Lys5Asn) rs104894361
NM_033360.4(KRAS):c.173C>T (p.Thr58Ile) rs104894364
NM_033360.4(KRAS):c.178G>A (p.Gly60Ser) rs104894359
NM_033360.4(KRAS):c.178G>C (p.Gly60Arg) rs104894359
NM_033360.4(KRAS):c.182A>G (p.Gln61Arg) rs121913240
NM_033360.4(KRAS):c.211T>C (p.Tyr71His) rs387907205
NM_033360.4(KRAS):c.214A>T (p.Met72Leu) rs727504662
NM_033360.4(KRAS):c.40G>A (p.Val14Ile) rs104894365
NM_033360.4(KRAS):c.439A>G (p.Lys147Glu) rs387907206
NM_033360.4(KRAS):c.440A>G (p.Lys147Arg) rs1135401776
NM_033360.4(KRAS):c.64C>G (p.Gln22Glu) rs121913236
NM_033360.4(KRAS):c.65A>G (p.Gln22Arg) rs727503110

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