"Counsyl"[submitter] AND "STK11"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 548908	NM_000455.5(STK11):c.56C>T (p.Ser19Leu)	STK11 (S19L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 237806	NM_000455.5(STK11):c.94A>G (p.Thr32Ala)	STK11 (T32A)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +3 more	GUncertain significance
Select item 135930	NM_000455.5(STK11):c.96C>G (p.Thr32=)	STK11	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 237791	NM_000455.5(STK11):c.120C>T (p.Arg40=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 403781	NM_000455.5(STK11):c.125G>T (p.Arg42Leu)	STK11 (R42L)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +3 more	GConflicting classifications of pathogenicity
Select item 7445	NM_000455.5(STK11):c.200T>C (p.Leu67Pro)	STK11 (L67P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 184178	NM_000455.5(STK11):c.237C>T (p.Ile79=)	STK11	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 548920	NM_000455.5(STK11):c.290+21_290+26dup	STK11	Duplication (intron variant)	not specified +2 more	GLikely benign
Select item 371854	NM_000455.5(STK11):c.290+22C>T	STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome	GLikely benign
Select item 182905	NM_000455.5(STK11):c.310A>G (p.Arg104Gly)	STK11 (R104G)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 185346	NM_000455.5(STK11):c.318G>A (p.Arg106=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GBenign/Likely benign
Select item 182877	NM_000455.5(STK11):c.357C>T (p.Asn119=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 184285	NM_000455.5(STK11):c.366G>A (p.Lys122=)	STK11	Single nucleotide variant (synonymous variant)	not specified +4 more	GBenign/Likely benign
Select item 548854	NM_000455.5(STK11):c.374+2T>C	STK11	Single nucleotide variant (splice donor variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 182878	NM_000455.5(STK11):c.374+11C>T	STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome +3 more	GConflicting classifications of pathogenicity
Select item 139330	NM_000455.5(STK11):c.375-7G>A	STK11	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 372048	NM_000455.5(STK11):c.375-5C>T	STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome	GConflicting classifications of pathogenicity
Select item 182906	NM_000455.5(STK11):c.397G>A (p.Val133Met)	STK11 (V133M)	Single nucleotide variant (missense variant)	Hepatoblastoma +4 more	GConflicting classifications of pathogenicity
Select item 183815	NM_000455.5(STK11):c.432G>A (p.Pro144=)	STK11	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 135920	NM_000455.5(STK11):c.434A>G (p.Glu145Gly)	STK11 (E145G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 216431	NM_000455.5(STK11):c.439C>T (p.Arg147Cys)	STK11 (R147C)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 141508	NM_000455.5(STK11):c.449T>C (p.Val150Ala)	STK11 (V150A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 403768	NM_000455.5(STK11):c.464+3G>A	STK11	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 216432	NM_000455.5(STK11):c.464+8C>T	STK11	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 142410	NM_000455.5(STK11):c.464+10C>T	STK11	Single nucleotide variant (intron variant)	Breast and/or ovarian cancer +7 more	GBenign/Likely benign
Select item 182879	NM_000455.5(STK11):c.464+20del	STK11	Deletion (intron variant)	Peutz-Jeghers syndrome +2 more	GBenign/Likely benign
Select item 139332	NM_000455.5(STK11):c.465-18G>T	STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome +3 more	GBenign/Likely benign
Select item 548867	NM_000455.5(STK11):c.465-17GT[2]	STK11	Microsatellite (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 219938	NM_000455.5(STK11):c.465-7C>T	STK11	Single nucleotide variant (intron variant)	not provided +3 more	GLikely benign
Select item 142034	NM_000455.5(STK11):c.465-5C>T	STK11	Single nucleotide variant (intron variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 127703	NM_000455.5(STK11):c.465-4G>A	STK11	Single nucleotide variant (intron variant)	Breast carcinoma +5 more	GConflicting classifications of pathogenicity
Select item 187230	NM_000455.5(STK11):c.537G>A (p.Pro179=)	STK11	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 141815	NM_000455.5(STK11):c.559G>A (p.Gly187Ser)	STK11 (G187S)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 141128	NM_000455.5(STK11):c.566C>T (p.Thr189Ile)	STK11 (T189I)	Single nucleotide variant (missense variant)	Carcinoma of pancreas +6 more	GConflicting classifications of pathogenicity
Select item 184001	NM_000455.5(STK11):c.594C>T (p.Ala198=)	STK11	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 328230	NM_000455.5(STK11):c.597+21dup	STK11	Duplication (intron variant)	Peutz-Jeghers syndrome +4 more	GBenign/Likely benign
Select item 182881	NM_000455.5(STK11):c.597+14del	STK11	Deletion (intron variant)	not specified +4 more	GBenign/Likely benign
Select item 548771	NM_000455.5(STK11):c.597+15G>T	STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome	GLikely benign
Select item 142394	NM_000455.5(STK11):c.598-11C>T	STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome +1 more	GConflicting classifications of pathogenicity
Select item 215740	NM_000455.5(STK11):c.598-7G>A	STK11	Single nucleotide variant (intron variant)	Breast and/or ovarian cancer +4 more	GBenign/Likely benign
Select item 182909	NM_000455.5(STK11):c.613G>A (p.Ala205Thr)	STK11 (A205T)	Single nucleotide variant (missense variant)	Melanoma, cutaneous malignant, susceptibility to, 1 +4 more	GConflicting classifications of pathogenicity
Select item 142443	NM_000455.5(STK11):c.614C>T (p.Ala205Val)	STK11 (A205V)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 182882	NM_000455.5(STK11):c.615G>A (p.Ala205=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +4 more	GBenign/Likely benign
Select item 184032	NM_000455.5(STK11):c.617C>T (p.Ala206Val)	STK11 (A206V)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 142319	NM_000455.5(STK11):c.618G>A (p.Ala206=)	STK11	Single nucleotide variant (synonymous variant)	Breast and/or ovarian cancer +4 more	GConflicting classifications of pathogenicity
Select item 184016	NM_000455.5(STK11):c.621C>T (p.Asp207=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 184313	NM_000455.5(STK11):c.631C>T (p.Arg211Trp)	STK11 (R211W)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 182910	NM_000455.5(STK11):c.632G>A (p.Arg211Gln)	STK11 (R211Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 183713	NM_000455.5(STK11):c.666C>T (p.Pro222=)	STK11	Single nucleotide variant (synonymous variant)	Breast and/or ovarian cancer +4 more	GBenign/Likely benign
Select item 184220	NM_000455.5(STK11):c.678C>T (p.Asn226=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 135926	NM_000455.5(STK11):c.721G>A (p.Ala241Thr)	STK11 (A241T)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance
Select item 135927	NM_000455.5(STK11):c.723T>C (p.Ala241=)	STK11	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign/Likely benign
Select item 234417	NM_000455.5(STK11):c.734+11C>T	STK11	Single nucleotide variant (intron variant)	not provided +2 more	GLikely benign
Select item 182884	NM_000455.5(STK11):c.734+19dup	STK11	Duplication (intron variant)	Peutz-Jeghers syndrome +2 more	GConflicting classifications of pathogenicity
Select item 492553	NM_000455.5(STK11):c.734+17C>A	STK11	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 139334	NM_000455.5(STK11):c.734+20G>A	STK11	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 371891	NM_000455.5(STK11):c.735-19C>T	STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome	GLikely benign
Select item 371789	NM_000455.5(STK11):c.735-6_735-2del	STK11	Deletion (splice acceptor variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 139335	NM_000455.5(STK11):c.787T>C (p.Leu263=)	STK11	Single nucleotide variant (synonymous variant)	not specified +4 more	GBenign/Likely benign
Select item 182885	NM_000455.5(STK11):c.795G>A (p.Glu265=)	STK11	Single nucleotide variant (synonymous variant)	Breast and/or ovarian cancer +4 more	GBenign/Likely benign
Select item 184316	NM_000455.5(STK11):c.828C>T (p.Gly276=)	STK11	Single nucleotide variant (synonymous variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 371980	NM_000455.5(STK11):c.836_837delinsCT (p.Gly279Ala)	STK11 (G279A)	Indel (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 142115	NM_000455.5(STK11):c.842C>T (p.Pro281Leu)	STK11 (P281L)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +5 more	GConflicting classifications of pathogenicity
Select item 371968	NM_000455.5(STK11):c.862+23C>T	STK11	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 378679	NM_000455.5(STK11):c.863-6C>T	STK11	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 182886	NM_000455.5(STK11):c.876C>T (p.Tyr292=)	STK11	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 216435	NM_000455.5(STK11):c.902G>A (p.Arg301Gln)	STK11 (R301Q)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 127709	NM_000455.5(STK11):c.920+5G>A	STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome +3 more	GConflicting classifications of pathogenicity
Select item 371810	NM_000455.5(STK11):c.920+7_920+8delinsCA	STK11	Indel (intron variant)	Peutz-Jeghers syndrome +1 more	GConflicting classifications of pathogenicity
Select item 215742	NM_000455.5(STK11):c.920+7G>A	STK11	Single nucleotide variant (intron variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 548716	NM_000455.5(STK11):c.920+28C>T	STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome	GLikely benign
Select item 371871	NM_000455.5(STK11):c.920+29G>A	STK11	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 256208	NM_000455.5(STK11):c.920+32G>A	STK11	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 139338	NM_000455.5(STK11):c.921-10G>A	STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome +3 more	GBenign/Likely benign
Select item 215743	NM_000455.5(STK11):c.921-8G>A	STK11	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 237807	NM_000455.5(STK11):c.957A>G (p.Pro319=)	STK11	Single nucleotide variant (synonymous variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 127710	NM_000455.5(STK11):c.970C>G (p.Pro324Ala)	STK11 (P324A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 184692	NM_000455.5(STK11):c.976C>A (p.Pro326Thr)	STK11 (P326T)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 220714	NM_000455.5(STK11):c.980A>G (p.Asp327Gly)	STK11 (D327G)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 141962	NM_000455.5(STK11):c.992G>A (p.Arg331Gln)	LOC130062899, STK11 (R331Q)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 142198	NM_000455.5(STK11):c.1012G>A (p.Val338Met)	LOC130062899, STK11 (V338M)	Single nucleotide variant (missense variant)	Carcinoma of pancreas +6 more	GConflicting classifications of pathogenicity
Select item 183994	NM_000455.5(STK11):c.1035C>T (p.His345=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 184026	NM_000455.5(STK11):c.1038C>T (p.Gly346=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 141089	NM_000455.5(STK11):c.1039G>A (p.Ala347Thr)	LOC130062899, STK11 (A347T)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 184691	NM_000455.5(STK11):c.1041G>A (p.Ala347=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 184837	NM_000455.5(STK11):c.1062C>T (p.Phe354=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +2 more	GBenign/Likely benign
Select item 7461	NM_000455.5(STK11):c.1062C>G (p.Phe354Leu)	LOC130062899, STK11 (F354L)	Single nucleotide variant (missense variant)	Melanoma, cutaneous malignant, susceptibility to, 1 +7 more	GBenign/Likely benign
Select item 135277	NM_000455.5(STK11):c.1088C>T (p.Thr363Ile)	LOC130062899, STK11 (T363I)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +2 more	GConflicting classifications of pathogenicity
Select item 142939	NM_000455.5(STK11):c.1100C>T (p.Thr367Met)	LOC130062899, STK11 (T367M)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 548727	NM_000455.5(STK11):c.1109-21C>T	STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome	GLikely benign
Select item 378680	NM_000455.5(STK11):c.1109-14C>T	STK11	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 372045	NM_000455.5(STK11):c.1109-13G>A	STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome +2 more	GBenign/Likely benign
Select item 141797	NM_000455.5(STK11):c.1109-5C>T	STK11	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 127698	NM_000455.5(STK11):c.1127A>C (p.Glu376Ala)	STK11 (E376A)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +4 more	GConflicting classifications of pathogenicity
Select item 141991	NM_000455.5(STK11):c.1130C>T (p.Ala377Val)	STK11 (A377V)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +2 more	GConflicting classifications of pathogenicity
Select item 184504	NM_000455.5(STK11):c.1137C>T (p.His379=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +1 more	GBenign/Likely benign
Select item 234419	NM_000455.5(STK11):c.1150C>T (p.Arg384Trp)	STK11 (R384W)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 142537	NM_000455.5(STK11):c.1151G>A (p.Arg384Gln)	STK11 (R384Q)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 142283	NM_000455.5(STK11):c.1168G>A (p.Val390Met)	STK11 (V390M)	Single nucleotide variant (missense variant)	Ovarian cancer +4 more	GConflicting classifications of pathogenicity
Select item 216427	NM_000455.5(STK11):c.1174A>G (p.Met392Val)	STK11 (M392V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity

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