ClinVar for Gene (Select 3845) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065766	NM_033360.4(KRAS):c.490C>T (p.Arg164Ter)	KRAS (R164*)	Single nucleotide variant (nonsense +1 more)	Carcinoma of pancreas	GLikely pathogenic
Select item 3063250	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835641)x3	A2M, A2ML1 +278 more	Copy number gain	not specified	GPathogenic
Select item 3061523	NM_004985.5(KRAS):c.-167A>C	KRAS, LOC130007561	Single nucleotide variant (5 prime UTR variant)	KRAS-related condition	GLikely benign
Select item 3046122	NM_004985.5(KRAS):c.-169_-149del	KRAS, LOC130007561	Deletion (5 prime UTR variant)	KRAS-related condition	GLikely benign
Select item 3023757	NM_004985.5(KRAS):c.450+3A>G	KRAS	Single nucleotide variant (intron variant)	RASopathy	GUncertain significance
Select item 3009878	NM_004985.5(KRAS):c.548C>G (p.Thr183Arg)	KRAS (T183R)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 2994655	NM_004985.5(KRAS):c.261T>G (p.Thr87=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy	GLikely benign
Select item 2914356	NM_004985.5(KRAS):c.550_551del (p.Lys184fs)	KRAS (K184fs)	Deletion (3 prime UTR variant +1 more)	RASopathy	GUncertain significance
Select item 2909102	NM_004985.5(KRAS):c.331A>G (p.Met111Val)	KRAS (M111V)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 2908507	NM_004985.5(KRAS):c.451-12T>G	KRAS	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 2898010	NM_004985.5(KRAS):c.426T>A (p.Ile142=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy	GLikely benign
Select item 2896377	NM_004985.5(KRAS):c.136A>G (p.Ile46Val)	KRAS (I46V)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 2857742	NM_004985.5(KRAS):c.132A>G (p.Val44=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy	GLikely benign
Select item 2845472	NM_004985.5(KRAS):c.290+7T>A	KRAS	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 2828010	NM_004985.5(KRAS):c.202A>G (p.Arg68Gly)	KRAS (R68G)	Single nucleotide variant (missense variant)	RASopathy	GLikely pathogenic
Select item 2820207	NM_004985.5(KRAS):c.112-12C>G	KRAS	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 2819836	NM_004985.5(KRAS):c.510G>C (p.Met170Ile)	KRAS (M170I)	Single nucleotide variant (3 prime UTR variant +1 more)	RASopathy	GUncertain significance
Select item 2818268	NM_004985.5(KRAS):c.556G>A (p.Val186Ile)	KRAS (V186I)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 2799402	NM_004985.5(KRAS):c.225G>C (p.Gly75=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy	GUncertain significance
Select item 2772438	NM_004985.5(KRAS):c.373G>A (p.Val125Ile)	KRAS (V125I)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 2764234	NM_004985.5(KRAS):c.435A>T (p.Ser145=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy	GLikely benign
Select item 2763049	NM_004985.5(KRAS):c.112-20C>A	KRAS	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 2759640	NM_004985.5(KRAS):c.548C>A (p.Thr183Lys)	KRAS (T183K)	Single nucleotide variant (3 prime UTR variant +1 more)	RASopathy	GUncertain significance
Select item 2758762	NM_004985.5(KRAS):c.54C>T (p.Ala18=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy	GLikely benign
Select item 2755102	NM_004985.5(KRAS):c.465C>G (p.Ala155=)	KRAS	Single nucleotide variant (3 prime UTR variant +1 more)	RASopathy	GLikely benign
Select item 2752227	NM_004985.5(KRAS):c.441G>T (p.Lys147Asn)	KRAS (K147N)	Single nucleotide variant (missense variant)	RASopathy	GLikely pathogenic
Select item 2716407	NM_004985.5(KRAS):c.467T>C (p.Phe156Ser)	KRAS (F156S)	Single nucleotide variant (3 prime UTR variant +1 more)	RASopathy	GLikely pathogenic
Select item 2714298	NM_004985.5(KRAS):c.547A>G (p.Thr183Ala)	KRAS (T183A)	Single nucleotide variant (3 prime UTR variant +1 more)	RASopathy	GUncertain significance
Select item 2697277	NM_004985.5(KRAS):c.507G>A (p.Lys169=)	KRAS	Single nucleotide variant (3 prime UTR variant +1 more)	RASopathy	GLikely benign
Select item 2689336	NM_004985.5(KRAS):c.152G>C (p.Cys51Ser)	KRAS (C51S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2672092	NM_004985.5(KRAS):c.178_198dup (p.Ala66_Met67insGlyGlnGluGluTyrSerAla)	KRAS	Duplication (inframe_insertion)	Vascular malformation	GLikely pathogenic
Select item 2671607	Single allele	FGD4, FGF23 +278 more	Duplication	not provided	GPathogenic
Select item 2662065	NM_004985.5(KRAS):c.479T>G (p.Val160Gly)	KRAS (V160G)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2642799	NC_000012.12:g.25251441T>C	KRAS, LOC130007561	Single nucleotide variant	not provided	GBenign
Select item 2642798	NC_000012.12:g.25251300A>G	LOC130007561, KRAS	Single nucleotide variant	not provided	GLikely benign
Select item 2642797	NC_000012.12:g.25251295C>G	KRAS, LOC130007561	Single nucleotide variant	not provided	GBenign
Select item 2642796	NM_004985.5(KRAS):c.*1634A>G	KRAS	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 2642795	NM_004985.5(KRAS):c.*4059A>G	KRAS	Single nucleotide variant (3 prime UTR variant)	not provided	GLikely benign
Select item 2630513	NM_004985.5(KRAS):c.101C>A (p.Pro34Gln)	KRAS (P34Q)	Single nucleotide variant (missense variant)	KRAS-related condition	GLikely pathogenic
Select item 2581679	NM_033360.4(KRAS):c.461A>T (p.Asp154Val)	KRAS (D154V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2575733	NM_004985.5(KRAS):c.148A>C (p.Thr50Pro)	KRAS (T50P)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2568296	NM_004985.5(KRAS):c.69A>G (p.Leu23=)	KRAS	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 2506804	NM_004985.5(KRAS):c.98A>G (p.Asp33Gly)	KRAS (D33G)	Single nucleotide variant (missense variant)	RASopathy +1 more	GUncertain significance
Select item 2505054	NM_004985.5(KRAS):c.106A>G (p.Ile36Val)	KRAS (I36V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2503842	NM_004985.5(KRAS):c.20T>A (p.Val7Glu)	KRAS (V7E)	Single nucleotide variant (missense variant)	RASopathy	GLikely pathogenic
Select item 2498256	NM_004985.5(KRAS):c.187G>A (p.Glu63Lys)	KRAS (E63K)	Single nucleotide variant (missense variant)	Teratoma	GUncertain significance
Select item 2498003	NM_004985.5(KRAS):c.380C>G (p.Thr127Arg)	KRAS (T127R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2478131	NM_004985.5(KRAS):c.506A>G (p.Lys169Arg)	KRAS (K169R)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2454058	NM_004985.5(KRAS):c.348T>C (p.Asn116=)	KRAS	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 2454057	NM_004985.5(KRAS):c.168C>T (p.Leu56=)	KRAS	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 2445417	GRCh37/hg19 12p13.33-11.1(chr12:176047-34179852)x4	AKAP3, ETFRF1 +278 more	Copy number gain	Pallister-Killian syndrome	GPathogenic
Select item 2444789	NM_004985.5(KRAS):c.121A>G (p.Arg41Gly)	KRAS (R41G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2431456	NM_004985.5(KRAS):c.175_176delinsTT (p.Ala59Leu)	KRAS (A59L)	Indel (missense variant)	Cardiofaciocutaneous syndrome 2	GLikely pathogenic
Select item 2425255	NC_000012.11:g.(?_25362729)_(25362865_?)dup	KRAS	Duplication	RASopathy	GUncertain significance
Select item 2425254	NC_000012.11:g.(?_25398188)_(25398318_?)dup	KRAS	Duplication	RASopathy	GUncertain significance
Select item 2239063	NM_033360.4(KRAS):c.560T>C (p.Ile187Thr)	KRAS (I187T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2195758	NM_004985.5(KRAS):c.66G>A (p.Gln22=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy	GLikely benign
Select item 2189790	NM_004985.5(KRAS):c.438A>G (p.Ala146=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy	GLikely benign
Select item 2177694	NM_004985.5(KRAS):c.375A>G (p.Val125=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy	GLikely benign
Select item 2177432	NM_004985.5(KRAS):c.498T>C (p.His166=)	KRAS	Single nucleotide variant (3 prime UTR variant +1 more)	RASopathy	GLikely benign
Select item 2166346	NM_004985.5(KRAS):c.111+10G>A	KRAS	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 2156411	NM_004985.5(KRAS):c.141T>C (p.Asp47=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy +1 more	GLikely benign
Select item 2113755	NM_004985.5(KRAS):c.519_520inv (p.Gly174Ser)	KRAS (G174S)	Inversion (3 prime UTR variant +1 more)	RASopathy	GUncertain significance
Select item 2107036	NM_004985.5(KRAS):c.120C>T (p.Tyr40=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy	GLikely benign
Select item 2089677	NM_004985.5(KRAS):c.443C>G (p.Thr148Arg)	KRAS (T148R)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 2086297	NM_004985.5(KRAS):c.563T>C (p.Met188Thr)	KRAS (M188T)	Single nucleotide variant (3 prime UTR variant +1 more)	RASopathy	GUncertain significance
Select item 2061689	NM_004985.5(KRAS):c.283C>A (p.His95Asn)	KRAS (H95N)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 2039917	NM_004985.5(KRAS):c.290+11A>G	KRAS	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 2036506	NM_004985.5(KRAS):c.418C>T (p.Pro140Ser)	KRAS (P140S)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 2023985	NM_004985.5(KRAS):c.432A>G (p.Thr144=)	KRAS	Single nucleotide variant (synonymous variant)	RASopathy	GLikely benign
Select item 2010214	NM_004985.5(KRAS):c.13A>C (p.Lys5Gln)	KRAS (K5Q)	Single nucleotide variant (missense variant)	RASopathy	GLikely pathogenic
Select item 1990132	NM_004985.5(KRAS):c.105A>C (p.Thr35=)	KRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 1965797	NM_004985.5(KRAS):c.269T>A (p.Phe90Tyr)	KRAS (F90Y)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 1964996	NM_004985.5(KRAS):c.291-10dup	KRAS	Duplication (intron variant)	RASopathy	GBenign
Select item 1915455	NM_004985.5(KRAS):c.450+5G>A	KRAS	Single nucleotide variant (intron variant)	RASopathy	GUncertain significance
Select item 1908428	NM_004985.5(KRAS):c.325G>A (p.Val109Ile)	KRAS (V109I)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 1803998	NM_004985.5(KRAS):c.440A>T (p.Lys147Met)	KRAS (K147M)	Single nucleotide variant (missense variant)	Noonan syndrome 3	GLikely pathogenic
Select item 1803539	NM_004985.5(KRAS):c.283C>T (p.His95Tyr)	KRAS (H95Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1803471	NM_004985.5(KRAS):c.481C>T (p.Arg161Ter)	KRAS (R161*)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 1775477	NM_004985.5(KRAS):c.156C>T (p.Leu52=)	KRAS	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1774834	NM_004985.5(KRAS):c.153T>G (p.Cys51Trp)	KRAS (C51W)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1744676	NM_004985.5(KRAS):c.4A>C (p.Thr2Pro)	KRAS (T2P)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1742817	NM_004985.5(KRAS):c.474A>G (p.Thr158=)	KRAS	Single nucleotide variant (3 prime UTR variant +1 more)	Cardiovascular phenotype	GLikely benign
Select item 1734094	NM_004985.5(KRAS):c.36T>G (p.Gly12=)	KRAS	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1734090	NM_004985.5(KRAS):c.36T>A (p.Gly12=)	KRAS	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1732986	NM_004985.5(KRAS):c.358T>C (p.Leu120=)	KRAS	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1729613	NM_004985.5(KRAS):c.326T>A (p.Val109Glu)	KRAS (V109E)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1717054	NM_004985.5(KRAS):c.365C>G (p.Ser122Cys)	KRAS (S122C)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 1714092	NM_004985.5(KRAS):c.230G>T (p.Gly77Val)	KRAS (G77V)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 1711043	NM_004985.5(KRAS):c.111+16A>G	KRAS	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 1711042	NM_004985.5(KRAS):c.111+14del	KRAS	Deletion (intron variant)	RASopathy	GBenign
Select item 1711041	NM_004985.5(KRAS):c.99T>C (p.Asp33=)	KRAS	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711040	NM_004985.5(KRAS):c.95A>C (p.Tyr32Ser)	KRAS (Y32S)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711039	NM_004985.5(KRAS):c.91G>T (p.Glu31Ter)	KRAS (E31*)	Single nucleotide variant (nonsense)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711038	NM_004985.5(KRAS):c.111+11T>C	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711037	NM_004985.5(KRAS):c.90C>A (p.Asp30Glu)	KRAS (D30E)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711036	NM_004985.5(KRAS):c.9dup (p.Tyr4fs)	KRAS (Y4fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711035	NM_004985.5(KRAS):c.84T>A (p.Phe28Leu)	KRAS (F28L)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711034	NM_004985.5(KRAS):c.84del (p.Phe28fs)	KRAS (F28fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711033	NM_004985.5(KRAS):c.80A>T (p.His27Leu)	KRAS (H27L)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance

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