STK11[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1334888	t(17;19)(q25.1;p13.3)	STK11	Translocation	Adrenal cortex carcinoma	GUncertain significance
Select item 1701346	NC_000019.10:g.1201926G>A	STK11	Single nucleotide variant	not provided	GLikely benign
Select item 328202	NM_000455.5(STK11):c.-1098G>A	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 892102	NM_000455.5(STK11):c.-1097G>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 3231731	NM_000455.5(STK11):c.-1089_290+816dup	STK11	Duplication (splice donor variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 328205	NM_000455.5(STK11):c.-925C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 892103	NM_000455.5(STK11):c.-893C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 892104	NM_000455.5(STK11):c.-835C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 892105	NM_000455.5(STK11):c.-806C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 892106	NM_000455.5(STK11):c.-783G>A	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 892107	NM_000455.5(STK11):c.-775G>A	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 888657	NM_000455.5(STK11):c.-774C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 328206	NM_000455.5(STK11):c.-723G>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 328207	NM_000455.5(STK11):c.-635del	STK11	Deletion (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 888658	NM_000455.5(STK11):c.-590C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 328208	NM_000455.5(STK11):c.-587G>C	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 888659	NM_000455.5(STK11):c.-580G>A	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GBenign
Select item 328209	NM_000455.5(STK11):c.-577C>T	STK11	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GBenign
Select item 328210	NM_000455.5(STK11):c.-562G>C	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GBenign
Select item 803510	NM_000455.5(STK11):c.-551C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GLikely benign
Select item 328211	NM_000455.5(STK11):c.-546G>A	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 328212	NM_000455.5(STK11):c.-520C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 888660	NM_000455.5(STK11):c.-474G>A	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 328213	NM_000455.5(STK11):c.-461G>A	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GConflicting classifications of pathogenicity
Select item 328214	NM_000455.5(STK11):c.-447C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 328215	NM_000455.5(STK11):c.-430C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome +1 more	GBenign/Likely benign
Select item 890362	NM_000455.5(STK11):c.-388C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 328216	NM_000455.5(STK11):c.-387C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 890363	NM_000455.5(STK11):c.-333G>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 328217	NM_000455.5(STK11):c.-311C>T	STK11	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GBenign/Likely benign
Select item 890364	NM_000455.5(STK11):c.-302G>A	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 803511	NM_000455.5(STK11):c.-280C>A	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GLikely benign
Select item 328218	NM_000455.5(STK11):c.-274C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GBenign
Select item 328219	NM_000455.5(STK11):c.-229C>G	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 328220	NM_000455.5(STK11):c.-216A>C	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 328221	NM_000455.5(STK11):c.-193C>G	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 803512	NM_000455.5(STK11):c.-167C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GLikely benign
Select item 890921	NM_000455.5(STK11):c.-150G>A	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 328222	NM_000455.5(STK11):c.-137C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GBenign/Likely benign
Select item 890922	NM_000455.5(STK11):c.-136C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 890923	NM_000455.5(STK11):c.-128G>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 328223	NM_000455.5(STK11):c.-127T>C	STK11	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GBenign/Likely benign
Select item 328224	NM_000455.5(STK11):c.-107dup	STK11	Duplication (5 prime UTR variant)	Peutz-Jeghers syndrome	GConflicting classifications of pathogenicity
Select item 328225	NM_000455.5(STK11):c.-106C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 803513	NM_000455.5(STK11):c.-99C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GLikely benign
Select item 803514	NM_000455.5(STK11):c.-95G>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GLikely benign
Select item 328226	NM_000455.5(STK11):c.-81A>G	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 328227	NM_000455.5(STK11):c.-55C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 421099	NM_000455.5(STK11):c.-50_-43del	STK11	Deletion (5 prime UTR variant)	not specified	GLikely benign
Select item 379512	NM_000455.5(STK11):c.-49A>C	STK11	Single nucleotide variant (5 prime UTR variant)	not specified	GBenign
Select item 1290978	NM_000455.5(STK11):c.-48C>T	STK11	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 387617	NM_000455.5(STK11):c.-48C>G	STK11	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 385934	NM_000455.5(STK11):c.-19C>T	STK11	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 507127	NM_000455.5(STK11):c.-17A>G	STK11	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 628245	NM_000455.5(STK11):c.-16G>A	STK11	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 507780	NM_000455.5(STK11):c.-11del	STK11	Deletion (5 prime UTR variant)	Peutz-Jeghers syndrome +1 more	GConflicting classifications of pathogenicity
Select item 1332211	NM_000455.5(STK11):c.-12C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 383932	NM_000455.5(STK11):c.-11C>T	STK11	Single nucleotide variant (5 prime UTR variant)	not specified +2 more	GLikely benign
Select item 583838	NC_000019.9:g.(?_1206903)_(1207212_?)dup	STK11	Duplication	Peutz-Jeghers syndrome	GUncertain significance
Select item 385458	NM_000455.5(STK11):c.-10T>G	STK11	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 630396	NM_000455.5(STK11):c.-9G>A	STK11	Single nucleotide variant (5 prime UTR variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 422225	NM_000455.5(STK11):c.-7del	STK11	Deletion (5 prime UTR variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 926194	NM_000455.5(STK11):c.-6T>A	STK11	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 527862	NC_000019.9:g.(?_1206907)_(1207208_?)dup	STK11	Duplication	Peutz-Jeghers syndrome	GUncertain significance
Select item 186562	NM_000455.5(STK11):c.-5C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 627831	NM_000455.5(STK11):c.-4C>T	STK11	Single nucleotide variant (5 prime UTR variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
Select item 328228	NM_000455.5(STK11):c.-2G>T	STK11	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 185127	NM_000455.5(STK11):c.-1C>T	STK11	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 1707938	NM_000455.5(STK11):c.1A>G (p.Met1Val)	STK11 (M1V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 925776	NM_000455.5(STK11):c.1A>T (p.Met1Leu)	STK11 (M1L)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 649900	NM_000455.5(STK11):c.4G>C (p.Glu2Gln)	STK11 (E2Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2759809	NM_000455.5(STK11):c.5A>G (p.Glu2Gly)	STK11 (E2G)	Single nucleotide variant (missense variant +1 more)	Peutz-Jeghers syndrome	GUncertain significance
Select item 492547	NM_000455.5(STK11):c.5A>C (p.Glu2Ala)	STK11 (E2A)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +3 more	GUncertain significance
Select item 485011	NM_000455.5(STK11):c.6G>A (p.Glu2=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 458011	NM_000455.5(STK11):c.8TGG[1] (p.Val4del)	STK11 (V4del)	Microsatellite (inframe_deletion)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 920914	NM_000455.5(STK11):c.7G>C (p.Val3Leu)	STK11 (V3L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 419872	NM_000455.5(STK11):c.7G>A (p.Val3Met)	STK11 (V3M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 328229	NM_000455.5(STK11):c.8T>G (p.Val3Gly)	STK11 (V3G)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
Select item 527859	NM_000455.5(STK11):c.9G>A (p.Val3=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1051732	NM_000455.5(STK11):c.10G>C (p.Val4Leu)	STK11 (V4L)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
Select item 578236	NM_000455.5(STK11):c.10G>T (p.Val4Leu)	STK11 (V4L)	Single nucleotide variant (missense variant)	Melanoma, cutaneous malignant, susceptibility to, 1 +1 more	GUncertain significance
Select item 480709	NM_000455.5(STK11):c.10G>A (p.Val4Met)	STK11 (V4M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1747221	NM_000455.5(STK11):c.11T>G (p.Val4Gly)	STK11 (V4G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1042673	NM_000455.5(STK11):c.11T>C (p.Val4Ala)	STK11 (V4A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 2451999	NM_000455.5(STK11):c.12G>C (p.Val4=)	STK11	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 921128	NM_000455.5(STK11):c.12G>A (p.Val4=)	STK11	Single nucleotide variant (synonymous variant)	not specified +2 more	GLikely benign
Select item 1771767	NM_000455.5(STK11):c.13G>A (p.Asp5Asn)	STK11 (D5N)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
Select item 839522	NM_000455.5(STK11):c.14A>G (p.Asp5Gly)	STK11 (D5G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 184490	NM_000455.5(STK11):c.15C>T (p.Asp5=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 1403746	NM_000455.5(STK11):c.16C>T (p.Pro6Ser)	STK11 (P6S)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
Select item 651673	NM_000455.5(STK11):c.16C>A (p.Pro6Thr)	STK11 (P6T)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 943418	NM_000455.5(STK11):c.17C>T (p.Pro6Leu)	STK11 (P6L)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
Select item 647785	NM_000455.5(STK11):c.17C>G (p.Pro6Arg)	STK11 (P6R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1586962	NM_000455.5(STK11):c.18G>A (p.Pro6=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome	GLikely benign
Select item 658263	NM_000455.5(STK11):c.18_19delinsAA (p.Gln7Lys)	STK11 (Q7K)	Indel (missense variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 527851	NM_000455.5(STK11):c.18G>C (p.Pro6=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1378041	NM_000455.5(STK11):c.19C>T (p.Gln7Ter)	STK11 (Q7*)	Single nucleotide variant (nonsense)	Peutz-Jeghers syndrome	GPathogenic
Select item 1516716	NM_000455.5(STK11):c.20A>G (p.Gln7Arg)	STK11 (Q7R)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 2002561	NM_000455.5(STK11):c.22C>A (p.Gln8Lys)	STK11 (Q8K)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 527816	NM_000455.5(STK11):c.22C>G (p.Gln8Glu)	STK11 (Q8E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance

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