"Genome-Nilou Lab"[submitter] AND "STK11"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 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
Select item 234549	NM_000455.5(STK11):c.25C>G (p.Leu9Val)	STK11 (L9V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GUncertain significance
Select item 927300	NM_000455.5(STK11):c.26T>A (p.Leu9Gln)	STK11 (L9Q)	Single nucleotide variant (missense variant)	Melanoma, cutaneous malignant, susceptibility to, 1 +2 more	GUncertain significance
Select item 573702	NM_000455.5(STK11):c.31A>T (p.Met11Leu)	STK11 (M11L)	Single nucleotide variant (missense variant)	See cases +3 more	GUncertain significance
Select item 233673	NM_000455.5(STK11):c.31A>G (p.Met11Val)	STK11 (M11V)	Single nucleotide variant (missense variant)	Melanoma, cutaneous malignant, susceptibility to, 1 +3 more	GUncertain significance
Select item 230472	NM_000455.5(STK11):c.33G>T (p.Met11Ile)	STK11 (M11I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 662432	NM_000455.5(STK11):c.38C>T (p.Thr13Met)	STK11 (T13M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 185666	NM_000455.5(STK11):c.41A>G (p.Glu14Gly)	STK11 (E14G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 215738	NM_000455.5(STK11):c.42G>A (p.Glu14=)	STK11	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 403797	NM_000455.5(STK11):c.43G>A (p.Gly15Ser)	STK11 (G15S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 184033	NM_000455.5(STK11):c.45C>T (p.Gly15=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 458049	NM_000455.5(STK11):c.49C>G (p.Leu17Val)	STK11 (L17V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 142223	NM_000455.5(STK11):c.52A>C (p.Met18Leu)	STK11 (M18L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 480712	NM_000455.5(STK11):c.53T>C (p.Met18Thr)	STK11 (M18T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 825783	NM_000455.5(STK11):c.54G>T (p.Met18Ile)	STK11 (M18I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 480711	NM_000455.5(STK11):c.54G>A (p.Met18Ile)	STK11 (M18I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
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 184297	NM_000455.5(STK11):c.57G>C (p.Ser19=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 419256	NM_000455.5(STK11):c.61G>A (p.Gly21Ser)	STK11 (G21S)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 826447	NM_000455.5(STK11):c.64A>G (p.Met22Val)	STK11 (M22V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 826758	NM_000455.5(STK11):c.69C>G (p.Asp23Glu)	STK11 (D23E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 766544	NM_000455.5(STK11):c.69C>T (p.Asp23=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +1 more	GConflicting classifications of pathogenicity
Select item 628078	NM_000455.5(STK11):c.71C>G (p.Thr24Arg)	STK11 (T24R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 403777	NM_000455.5(STK11):c.71C>T (p.Thr24Met)	STK11 (T24M)	Single nucleotide variant (missense variant)	Melanoma, cutaneous malignant, susceptibility to, 1 +3 more	GConflicting classifications of pathogenicity
Select item 378674	NM_000455.5(STK11):c.84C>T (p.Arg28=)	STK11	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 480723	NM_000455.5(STK11):c.90C>G (p.Asp30Glu)	STK11 (D30E)	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 141018	NM_000455.5(STK11):c.103A>G (p.Ile35Val)	STK11 (I35V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 486991	NM_000455.5(STK11):c.107A>G (p.Tyr36Cys)	STK11 (Y36C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 376334	NM_000455.5(STK11):c.109C>T (p.Gln37Ter)	STK11 (Q37*)	Single nucleotide variant (nonsense)	not provided +2 more	GPathogenic
Select item 628125	NM_000455.5(STK11):c.110A>G (p.Gln37Arg)	STK11 (Q37R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 458014	NM_000455.5(STK11):c.112C>G (p.Pro38Ala)	STK11 (P38A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 639482	NM_000455.5(STK11):c.113C>G (p.Pro38Arg)	STK11 (P38R)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 570301	NM_000455.5(STK11):c.113C>T (p.Pro38Leu)	STK11 (P38L)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +3 more	GUncertain significance
Select item 230795	NM_000455.5(STK11):c.115C>T (p.Arg39Cys)	STK11 (R39C)	Single nucleotide variant (missense variant)	Melanoma, cutaneous malignant, susceptibility to, 1 +2 more	GUncertain significance
Select item 480722	NM_000455.5(STK11):c.116G>A (p.Arg39His)	STK11 (R39H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 186826	NM_000455.5(STK11):c.116G>T (p.Arg39Leu)	STK11 (R39L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
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 568966	NM_000455.5(STK11):c.121A>C (p.Lys41Gln)	STK11 (K41Q)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
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 234700	NM_000455.5(STK11):c.125G>A (p.Arg42Gln)	STK11 (R42Q)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 486522	NM_000455.5(STK11):c.128C>T (p.Ala43Val)	STK11 (A43V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 505434	NM_000455.5(STK11):c.143A>G (p.Lys48Arg)	STK11 (K48R)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 182914	NM_000455.5(STK11):c.151A>C (p.Met51Leu)	STK11 (M51L)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +3 more	GUncertain significance
Select item 428751	NM_000455.5(STK11):c.155_157del (p.Gly52del)	STK11 (G52del)	Deletion (inframe_deletion)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 403765	NM_000455.5(STK11):c.156G>T (p.Gly52=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 93096	NM_000455.5(STK11):c.169dup (p.Glu57fs)	STK11 (E57fs)	Duplication (frameshift variant)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 234416	NM_000455.5(STK11):c.179dup (p.Tyr60Ter)	STK11 (Y60*)	Duplication (nonsense)	Peutz-Jeghers syndrome +1 more	GPathogenic/Likely pathogenic
Select item 503650	NM_000455.5(STK11):c.180del (p.Ser59_Tyr60insTer)	STK11	Deletion (nonsense)	Peutz-Jeghers syndrome +2 more	GPathogenic
Select item 428750	NM_000455.5(STK11):c.180C>A (p.Tyr60Ter)	STK11 (Y60*)	Single nucleotide variant (nonsense)	Peutz-Jeghers syndrome +1 more	GPathogenic
Select item 428749	NM_000455.5(STK11):c.180C>G (p.Tyr60Ter)	STK11 (Y60*)	Single nucleotide variant (nonsense)	Peutz-Jeghers syndrome +1 more	GPathogenic
Select item 439303	NM_000455.5(STK11):c.189G>A (p.Val63=)	STK11	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 638819	NM_000455.5(STK11):c.196G>A (p.Val66Met)	STK11 (V66M)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
Select item 439304	NM_000455.5(STK11):c.199del (p.Leu67fs)	STK11	Deletion (frameshift variant)	Peutz-Jeghers syndrome +1 more	GPathogenic/Likely pathogenic
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 856338	NM_000455.5(STK11):c.206C>T (p.Ser69Leu)	STK11 (S69L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 484998	NM_000455.5(STK11):c.206C>G (p.Ser69Trp)	STK11 (S69W)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
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 428763	NM_000455.5(STK11):c.238C>G (p.Leu80Val)	STK11 (L80V)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +2 more	GUncertain significance
Select item 922036	NM_000455.5(STK11):c.241A>C (p.Lys81Gln)	STK11 (K81Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 480725	NM_000455.5(STK11):c.242A>C (p.Lys81Thr)	STK11 (K81T)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
Select item 234584	NM_000455.5(STK11):c.248A>G (p.Lys83Arg)	STK11 (K83R)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +2 more	GConflicting classifications of pathogenicity
Select item 7443	NM_000455.5(STK11):c.250A>T (p.Lys84Ter)	STK11 (K84*)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic
Select item 93097	NM_000455.5(STK11):c.264C>A (p.Ile88=)	STK11	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign
Select item 821590	NM_000455.5(STK11):c.265C>T (p.Pro89Ser)	STK11 (P89S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 821799	NM_000455.5(STK11):c.277G>A (p.Ala93Thr)	STK11 (A93T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 229978	NM_000455.5(STK11):c.286A>G (p.Lys96Glu)	STK11 (K96E)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 141902	NM_000455.5(STK11):c.290+4_290+7del	STK11	Microsatellite (splice donor variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 428787	NM_000455.5(STK11):c.290+1G>A	STK11	Single nucleotide variant (splice donor variant)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic
Select item 256203	NM_000455.5(STK11):c.290+36G>T	STK11	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 127702	NM_000455.5(STK11):c.291-18_291-17del	STK11	Deletion (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 230469	NM_000455.5(STK11):c.291-2A>G	STK11	Single nucleotide variant (splice acceptor variant)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic
Select item 142382	NM_000455.5(STK11):c.297T>G (p.Ile99Met)	STK11 (I99M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 527836	NM_000455.5(STK11):c.298C>G (p.Gln100Glu)	STK11 (Q100E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 403771	NM_000455.5(STK11):c.299A>G (p.Gln100Arg)	STK11 (Q100R)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +4 more	GUncertain significance
Select item 135919	NM_000455.5(STK11):c.301C>G (p.Leu101Val)	STK11 (L101V)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +2 more	GConflicting classifications of pathogenicity
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 142871	NM_000455.5(STK11):c.310A>T (p.Arg104Trp)	STK11 (R104W)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +2 more	GUncertain significance
Select item 220485	NM_000455.5(STK11):c.312G>C (p.Arg104Ser)	STK11 (R104S)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +3 more	GUncertain significance
Select item 141922	NM_000455.5(STK11):c.316C>T (p.Arg106Trp)	STK11 (R106W)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 420770	NM_000455.5(STK11):c.317G>A (p.Arg106Gln)	STK11 (R106Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 216430	NM_000455.5(STK11):c.317G>T (p.Arg106Leu)	STK11 (R106L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 706134	NM_000455.5(STK11):c.327T>C (p.Asn109=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +2 more	GBenign/Likely benign
Select item 185602	NM_000455.5(STK11):c.334C>G (p.Gln112Glu)	STK11 (Q112E)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
Select item 527824	NM_000455.5(STK11):c.336G>C (p.Gln112His)	STK11 (Q112H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 492524	NM_000455.5(STK11):c.337C>G (p.Leu113Val)	STK11 (L113V)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1162090	NM_000455.5(STK11):c.345T>C (p.Asp115=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +2 more	GConflicting classifications of pathogenicity
Select item 412539	NM_000455.5(STK11):c.348G>T (p.Val116=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 219451	NM_000455.5(STK11):c.355A>G (p.Asn119Asp)	STK11 (N119D)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +2 more	GConflicting classifications of pathogenicity
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 490165	NM_000455.5(STK11):c.358G>A (p.Glu120Lys)	STK11 (E120K)	Single nucleotide variant (missense variant)	Carcinoma of pancreas +5 more	GUncertain significance

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