"All of Us Research Program, National Institutes of Health"[submitter] - ClinVar

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Items: 39

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 182889	NM_000455.5(STK11):c.984C>G (p.Thr328=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 230490	NM_000455.5(STK11):c.991C>T (p.Arg331Trp)	LOC130062899, STK11 (R331W)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 237785	NM_000455.5(STK11):c.1008T>C (p.Thr336=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
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 2774543	NM_000455.5(STK11):c.1014G>A (p.Val338=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 186311	NM_000455.5(STK11):c.1015C>G (p.Pro339Ala)	LOC130062899, STK11 (P339A)	Single nucleotide variant (missense variant)	Melanoma, cutaneous malignant, susceptibility to, 1 +4 more	GUncertain significance
Select item 142696	NM_000455.5(STK11):c.1016C>T (p.Pro339Leu)	LOC130062899, STK11 (P339L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GUncertain significance
Select item 233233	NM_000455.5(STK11):c.1017G>A (p.Pro339=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 185804	NM_000455.5(STK11):c.1020C>T (p.Tyr340=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	not specified +2 more	GLikely benign
Select item 140986	NM_000455.5(STK11):c.1027G>A (p.Asp343Asn)	LOC130062899, STK11 (D343N)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 3072086	NM_000455.5(STK11):c.1028A>G (p.Asp343Gly)	LOC130062899, STK11 (D343G)	Single nucleotide variant (missense variant +1 more)	Peutz-Jeghers syndrome	GUncertain significance
Select item 458010	NM_000455.5(STK11):c.1029C>T (p.Asp343=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +1 more	GLikely benign
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 141886	NM_000455.5(STK11):c.1036G>A (p.Gly346Ser)	LOC130062899, STK11 (G346S)	Single nucleotide variant (missense variant)	not specified +2 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 578037	NM_000455.5(STK11):c.1040C>T (p.Ala347Val)	LOC130062899, STK11 (A347V)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 141851	NM_000455.5(STK11):c.1040C>G (p.Ala347Gly)	LOC130062899, STK11 (A347G)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +2 more	GUncertain significance
Select item 403761	NM_000455.5(STK11):c.1045GAGGAC[1] (p.349ED[1])	LOC130062899, STK11	Microsatellite (inframe_deletion)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 185970	NM_000455.5(STK11):c.1044C>T (p.Asp348=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	Breast and/or ovarian cancer +4 more	GLikely benign
Select item 230358	NM_000455.5(STK11):c.1049A>G (p.Asp350Gly)	LOC130062899, STK11 (D350G)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
Select item 184376	NM_000455.5(STK11):c.1050C>T (p.Asp350=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 484997	NM_000455.5(STK11):c.1051G>A (p.Glu351Lys)	LOC130062899, STK11 (E351K)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 184351	NM_000455.5(STK11):c.1056C>T (p.Asp352=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
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 412547	NM_000455.5(STK11):c.1068C>T (p.Ile356=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 198732	NM_000455.5(STK11):c.1069G>A (p.Glu357Lys)	LOC130062899, STK11 (E357K)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 412537	NM_000455.5(STK11):c.1071G>T (p.Glu357Asp)	LOC130062899, STK11 (E357D)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 576503	NM_000455.5(STK11):c.1079T>C (p.Ile360Thr)	LOC130062899, STK11 (I360T)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome	GUncertain significance
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 822143	NM_000455.5(STK11):c.1091A>G (p.Gln364Arg)	LOC130062899, STK11 (Q364R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 664864	NM_000455.5(STK11):c.1093G>A (p.Asp365Asn)	LOC130062899, STK11 (D365N)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
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 185935	NM_000455.5(STK11):c.1101G>A (p.Thr367=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +3 more	GBenign/Likely benign
Select item 486520	NM_000455.5(STK11):c.1102G>A (p.Val368Met)	LOC130062899, STK11 (V368M)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +2 more	GUncertain significance
Select item 486523	NM_000455.5(STK11):c.1106C>G (p.Pro369Arg)	LOC130062899, STK11 (P369R)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
Select item 237786	NM_000455.5(STK11):c.1107C>T (p.Pro369=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +2 more	GLikely benign
Select item 185965	NM_000455.5(STK11):c.1108G>A (p.Gly370Arg)	LOC130062899, STK11 (G370R)	Single nucleotide variant (missense variant)	Melanoma, cutaneous malignant, susceptibility to, 1 +2 more	GUncertain significance
Select item 578710	NM_000455.5(STK11):c.1108+6T>C	LOC130062899, STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance

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Items: 39