List of variants in gene KRAS reported as likely pathogenic

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: 66

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.149C>T (p.Thr50Ile)	rs1407509439	0.00001
NM_004985.5(KRAS):c.35G>A (p.Gly12Asp)	rs121913529	0.00001
NM_004985.5(KRAS):c.38G>A (p.Gly13Asp)	rs112445441	0.00001
NM_004985.5(KRAS):c.57G>C (p.Leu19Phe)	rs121913538	0.00001
NM_004985.5(KRAS):c.101C>A (p.Pro34Gln)
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>C (p.Lys5Gln)
NM_004985.5(KRAS):c.13A>G (p.Lys5Glu)	rs193929331
NM_004985.5(KRAS):c.148A>C (p.Thr50Pro)
NM_004985.5(KRAS):c.173_214dup (p.Thr58_Tyr71dup)	rs2141509791
NM_004985.5(KRAS):c.175_176delinsTT (p.Ala59Leu)
NM_004985.5(KRAS):c.178_198dup (p.Ala66_Met67insGlyGlnGluGluTyrSerAla)
NM_004985.5(KRAS):c.179G>T (p.Gly60Val)	rs727503108
NM_004985.5(KRAS):c.182A>T (p.Gln61Leu)	rs121913240
NM_004985.5(KRAS):c.183A>C (p.Gln61His)	rs17851045
NM_004985.5(KRAS):c.183A>T (p.Gln61His)	rs17851045
NM_004985.5(KRAS):c.184GAG[1] (p.Glu63del)	rs730880469
NM_004985.5(KRAS):c.197_223dup (p.Ala66_Thr74dup)	rs2141509708
NM_004985.5(KRAS):c.202A>G (p.Arg68Gly)
NM_004985.5(KRAS):c.202_204del (p.Arg68del)	rs1951405809
NM_004985.5(KRAS):c.20T>A (p.Val7Glu)
NM_004985.5(KRAS):c.211T>G (p.Tyr71Asp)	rs387907205
NM_004985.5(KRAS):c.214A>C (p.Met72Leu)	rs727504662
NM_004985.5(KRAS):c.214A>T (p.Met72Leu)	rs727504662
NM_004985.5(KRAS):c.220A>C (p.Thr74Pro)	rs770020203
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.290G>A (p.Arg97Lys)	rs727503106
NM_004985.5(KRAS):c.346A>C (p.Asn116His)	rs2141506264
NM_004985.5(KRAS):c.34G>C (p.Gly12Arg)	rs121913530
NM_004985.5(KRAS):c.34G>T (p.Gly12Cys)	rs121913530
NM_004985.5(KRAS):c.35G>C (p.Gly12Ala)	rs121913529
NM_004985.5(KRAS):c.35G>T (p.Gly12Val)	rs121913529
NM_004985.5(KRAS):c.37G>T (p.Gly13Cys)	rs121913535
NM_004985.5(KRAS):c.38G>T (p.Gly13Val)	rs112445441
NM_004985.5(KRAS):c.39C>A (p.Gly13=)	rs397517040
NM_004985.5(KRAS):c.39C>T (p.Gly13=)	rs397517040
NM_004985.5(KRAS):c.436G>A (p.Ala146Thr)	rs121913527
NM_004985.5(KRAS):c.440A>T (p.Lys147Met)
NM_004985.5(KRAS):c.441G>T (p.Lys147Asn)
NM_004985.5(KRAS):c.445A>T (p.Arg149Ter)	rs2141505552
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.461A>G (p.Asp154Gly)	rs2141481712
NM_004985.5(KRAS):c.466T>G (p.Phe156Val)	rs397517042
NM_004985.5(KRAS):c.467T>C (p.Phe156Ser)
NM_033360.4(KRAS):c.15A>T (p.Lys5Asn)	rs104894361
NM_033360.4(KRAS):c.175G>A (p.Ala59Thr)	rs121913528
NM_033360.4(KRAS):c.175G>T (p.Ala59Ser)	rs121913528
NM_033360.4(KRAS):c.181C>G (p.Gln61Glu)	rs121913238
NM_033360.4(KRAS):c.182A>C (p.Gln61Pro)	rs121913240
NM_033360.4(KRAS):c.189G>C (p.Glu63Asp)	rs1592808357
NM_033360.4(KRAS):c.189G>T (p.Glu63Asp)	rs1592808357
NM_033360.4(KRAS):c.194G>T (p.Ser65Ile)	rs1555194026
NM_033360.4(KRAS):c.351A>C (p.Lys117Asn)	rs770248150
NM_033360.4(KRAS):c.355G>A (p.Asp119Asn)	rs730880471
NM_033360.4(KRAS):c.436G>C (p.Ala146Pro)	rs121913527
NM_033360.4(KRAS):c.436G>T (p.Ala146Ser)	rs121913527
NM_033360.4(KRAS):c.439A>G (p.Lys147Glu)	rs387907206
NM_033360.4(KRAS):c.44G>T (p.Gly15Val)	rs1555195579
NM_033360.4(KRAS):c.458A>C (p.Glu153Ala)	rs1592798693
NM_033360.4(KRAS):c.57G>T (p.Leu19Phe)	rs121913538
NM_033360.4(KRAS):c.64C>A (p.Gln22Lys)	rs121913236
NM_033360.4(KRAS):c.68T>G (p.Leu23Arg)	rs730880472

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