Related gene-specific medical variations for Gene (Select 3845) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3344430	NM_004985.5(KRAS):c.-158C>G	KRAS, LOC130007561	Single nucleotide variant (5 prime UTR variant)	KRAS-related disorder	GLikely benign
Select item 3244348	NC_000012.11:g.(?_25362729)_(25380366_?)dup	KRAS	Duplication	RASopathy	GUncertain significance
Select item 3244347	NC_000012.11:g.(?_25378528)_(25398318_?)dup	KRAS	Duplication	RASopathy	GUncertain significance
Select item 3238829	NM_004985.5(KRAS):c.202A>T (p.Arg68Trp)	KRAS (R68W)	Single nucleotide variant (missense variant)	Noonan syndrome 3	GLikely pathogenic
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 3061523	NM_004985.5(KRAS):c.-167A>C	KRAS, LOC130007561	Single nucleotide variant (5 prime UTR variant)	KRAS-related disorder	GLikely benign
Select item 3046122	NM_004985.5(KRAS):c.-169_-149del	KRAS, LOC130007561	Deletion (5 prime UTR variant)	KRAS-related disorder	GLikely benign
Select item 2672092	NM_004985.5(KRAS):c.178_198dup (p.Ala66_Met67insGlyGlnGluGluTyrSerAla)	KRAS	Duplication (inframe_insertion)	Vascular malformation	GLikely pathogenic
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
Select item 1711032	NM_004985.5(KRAS):c.80A>G (p.His27Arg)	KRAS (H27R)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711031	NM_004985.5(KRAS):c.77A>C (p.Asn26Thr)	KRAS (N26T)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711030	NM_004985.5(KRAS):c.75G>A (p.Gln25=)	KRAS	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711029	NM_004985.5(KRAS):c.74A>T (p.Gln25Leu)	KRAS (Q25L)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711028	NM_004985.5(KRAS):c.10T>A (p.Tyr4Asn)	KRAS (Y4N)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711027	NM_004985.5(KRAS):c.6T>G (p.Thr2=)	KRAS	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711026	NM_004985.5(KRAS):c.-6C>T	KRAS	Single nucleotide variant (5 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711025	NM_004985.5(KRAS):c.65A>C (p.Gln22Pro)	KRAS (Q22P)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711024	NM_004985.5(KRAS):c.62T>A (p.Ile21Lys)	KRAS (I21K)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711023	NM_004985.5(KRAS):c.5C>G (p.Thr2Ser)	KRAS (T2S)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711022	NM_004985.5(KRAS):c.50G>T (p.Ser17Ile)	KRAS (S17I)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711021	NM_004985.5(KRAS):c.4del (p.Thr2fs)	KRAS (T2fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711020	NM_004985.5(KRAS):c.43G>T (p.Gly15Cys)	KRAS (G15C)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711019	NM_004985.5(KRAS):c.42A>T (p.Val14=)	KRAS	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711018	NM_004985.5(KRAS):c.-10C>G	KRAS	Single nucleotide variant (5 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711017	NM_004985.5(KRAS):c.33T>A (p.Ala11=)	KRAS	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711016	NM_004985.5(KRAS):c.31G>T (p.Ala11Ser)	KRAS (A11S)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711015	NM_004985.5(KRAS):c.29_31del (p.Gly10del)	KRAS (G10del)	Deletion (inframe_deletion)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711014	NM_004985.5(KRAS):c.29_30insT (p.Ala11fs)	KRAS (A11fs)	Insertion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711013	NM_004985.5(KRAS):c.27T>G (p.Val9=)	KRAS	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711012	NM_004985.5(KRAS):c.27T>A (p.Val9=)	KRAS	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711011	NM_004985.5(KRAS):c.27_28insCTC (p.Val9_Gly10insLeu)	KRAS	Insertion (inframe_insertion)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711010	NM_004985.5(KRAS):c.24dup (p.Val9fs)	KRAS (V9fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711009	NM_004985.5(KRAS):c.21_22insT (p.Val8fs)	KRAS (V8fs)	Insertion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711008	NM_004985.5(KRAS):c.109G>T (p.Glu37Ter)	KRAS (E37*)	Single nucleotide variant (nonsense)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711007	NM_004985.5(KRAS):c.1del (p.Met1*)	KRAS	Deletion (nonsense +1 more)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711006	NM_004985.5(KRAS):c.16C>T (p.Leu6Phe)	KRAS (L6F)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711005	NM_004985.5(KRAS):c.13A>T (p.Lys5Ter)	KRAS (K5*)	Single nucleotide variant (nonsense)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711004	NM_004985.5(KRAS):c.12T>A (p.Tyr4Ter)	KRAS (Y4*)	Single nucleotide variant (nonsense)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711003	NM_004985.5(KRAS):c.-11G>A	KRAS	Single nucleotide variant (5 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711002	NM_033360.4(KRAS):c.-11delG	KRAS	Deletion (splice acceptor variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711001	NM_004985.5(KRAS):c.11A>T (p.Tyr4Phe)	KRAS (Y4F)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711000	NM_004985.5(KRAS):c.-11-8A>C	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710999	NM_004985.5(KRAS):c.-11-8_-11-7insC	KRAS	Insertion (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710998	NM_004985.5(KRAS):c.109_110insC (p.Glu37fs)	KRAS (E37fs)	Insertion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710997	NM_004985.5(KRAS):c.-11-7T>A	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710996	NM_004985.5(KRAS):c.-11-51del	KRAS	Deletion (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710995	NM_004985.5(KRAS):c.-11-4T>A	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710994	NM_004985.5(KRAS):c.-11-36C>T	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710993	NM_004985.5(KRAS):c.-11-2A>T	KRAS	Single nucleotide variant (splice acceptor variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710992	NM_004985.5(KRAS):c.-11-2A>C	KRAS	Single nucleotide variant (splice acceptor variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710991	NM_004985.5(KRAS):c.-11-21T>G	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710990	NM_004985.5(KRAS):c.-11-1G>C	KRAS	Single nucleotide variant (splice acceptor variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710989	NM_004985.5(KRAS):c.-11-12T>G	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710988	NM_004985.5(KRAS):c.-11-12T>A	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710987	NM_004985.5(KRAS):c.108delinsCC (p.Glu37fs)	KRAS (E37fs)	Indel (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710986	NM_004985.5(KRAS):c.-11-10T>G	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710985	NM_004985.5(KRAS):c.111+8T>C	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710984	NM_004985.5(KRAS):c.111+6T>C	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710983	NM_004985.5(KRAS):c.111+53A>G	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710982	NM_004985.5(KRAS):c.111+50T>A	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710981	NM_004985.5(KRAS):c.111+30G>T	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710980	NM_004985.5(KRAS):c.111+28C>T	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710979	NM_004985.5(KRAS):c.111+25T>C	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710978	NM_004985.5(KRAS):c.111+24A>G	KRAS	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710977	NM_004985.5(KRAS):c.111+1G>C	KRAS	Single nucleotide variant (splice donor variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1710976	NM_004985.5(KRAS):c.107T>A (p.Ile36Lys)	KRAS (I36K)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1701193	NM_004985.5(KRAS):c.33_34delinsCT (p.Gly12Cys)	KRAS (G12C)	Indel (missense variant)	not provided	GPathogenic
Select item 1676497	NM_004985.5(KRAS):c.229G>T (p.Gly77Cys)	KRAS (G77C)	Single nucleotide variant	Noonan syndrome 3	GLikely pathogenic
Select item 1334244	NM_004985.5(KRAS):c.-167_-153dup	KRAS, LOC130007561	Duplication (5 prime UTR variant)	Noonan syndrome and Noonan-related syndrome	GUncertain significance
Select item 1334243	NM_004985.5(KRAS):c.-14G>C	KRAS, LOC130007561	Single nucleotide variant (5 prime UTR variant +1 more)	Noonan syndrome and Noonan-related syndrome	GUncertain significance
Select item 1327505	NM_004985.5(KRAS):c.445A>T (p.Arg149Ter)	KRAS (R149*)	Single nucleotide variant (nonsense)	Thyroid cancer, nonmedullary, 1	GLikely pathogenic
Select item 1235060	NM_004985.5(KRAS):c.-190C>T	KRAS, LOC130007561	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1098601	NM_004985.5(KRAS):c.58A>G (p.Thr20Ala)	KRAS (T20A)	Single nucleotide variant (missense variant)	Cardiofaciocutaneous syndrome 2	GUncertain significance
Select item 931154	NM_004985.5(KRAS):c.534_536del (p.Lys180del)	KRAS (K180del)	Deletion (3 prime UTR variant +1 more)	Toriello-Lacassie-Droste syndrome	GUncertain significance
Select item 509071	NM_033360.4(KRAS):c.-44A>G	KRAS, LOC130007561	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 431103	NM_033360.4(KRAS):c.440A>G (p.Lys147Arg)	KRAS (K147R)	Single nucleotide variant (missense variant)	Noonan syndrome 3	GPathogenic
Select item 376324	NM_033360.4(KRAS):c.181C>G (p.Gln61Glu)	KRAS (Q61E)	Single nucleotide variant (missense variant)	Neoplasm of the large intestine	GLikely pathogenic
Select item 375968	NM_033360.4(KRAS):c.37G>A (p.Gly13Ser)	KRAS (G13S)	Single nucleotide variant (missense variant)	Neoplasm of the large intestine +2 more	GPathogenic
Select item 375967	NM_033360.4(KRAS):c.38G>C (p.Gly13Ala)	KRAS (G13A)	Single nucleotide variant (missense variant)	Neoplasm of the large intestine +1 more	GPathogenic
Select item 375966	NM_033360.4(KRAS):c.182A>C (p.Gln61Pro)	KRAS (Q61P)	Single nucleotide variant (missense variant)	Thyroid tumor +1 more	GPathogenic/Likely pathogenic
Select item 308127	NM_033360.4(KRAS):c.-180G>A	KRAS, LOC130007561	Single nucleotide variant (5 prime UTR variant)	Noonan syndrome	GUncertain significance
Select item 308126	NM_004985.5(KRAS):c.-176CGG[4]	KRAS, LOC130007561	Microsatellite (5 prime UTR variant)	Cardio-facio-cutaneous syndrome +1 more	GUncertain significance
Select item 308125	NM_033360.4(KRAS):c.-128C>G	KRAS, LOC130007561	Single nucleotide variant (5 prime UTR variant)	Noonan syndrome	GUncertain significance
Select item 262226	NM_004985.5(KRAS):c.451-5542C>T	KRAS	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 259601	NM_033360.4(KRAS):c.111+46T>G	KRAS	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 180715	NM_033360.4(KRAS):c.*37A>G	KRAS	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GBenign
Select item 177932	NM_004985.5(KRAS):c.-178C>A	KRAS, LOC130007561	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 177929	NM_033360.4(KRAS):c.-48_-29dup	KRAS, LOC130007561	Duplication (5 prime UTR variant)	not specified +1 more	GBenign/Likely benign
Select item 177893	NM_004985.5(KRAS):c.-148_-137del	KRAS, LOC130007561	Deletion	not specified	GUncertain significance
Select item 177710	NM_004985.5(KRAS):c.-122C>T	LOC130007561, KRAS	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GLikely benign
Select item 163772	NM_004985.5(KRAS):c.-167A>G	KRAS, LOC130007561	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 163771	NM_004985.5(KRAS):c.-160A>G	KRAS, LOC130007561	Single nucleotide variant (5 prime UTR variant)	RASopathy	GBenign FDA Recognized database

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