"Color Diagnostics, LLC DBA Color Health"[submitter] AND "STK11"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 provided +4 more	GConflicting classifications of pathogenicity
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 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 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 921128	NM_000455.5(STK11):c.12G>A (p.Val4=)	STK11	Single nucleotide variant (synonymous variant)	not specified +2 more	GLikely benign
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 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 923852	NM_000455.5(STK11):c.25C>T (p.Leu9=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
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 1332451	NM_000455.5(STK11):c.27G>A (p.Leu9=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +1 more	GLikely benign
Select item 573702	NM_000455.5(STK11):c.31A>T (p.Met11Leu)	STK11 (M11L)	Single nucleotide variant (missense variant)	not specified +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 490164	NM_000455.5(STK11):c.33_35del (p.Met11_Phe12delinsIle)	STK11	Deletion (inframe_indel)	Hereditary cancer-predisposing syndrome	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 2774532	NM_000455.5(STK11):c.42G>C (p.Glu14Asp)	STK11 (E14D)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	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 391105	NM_000455.5(STK11):c.48G>A (p.Glu16=)	STK11	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 458049	NM_000455.5(STK11):c.49C>G (p.Leu17Val)	STK11 (L17V)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +2 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)	Peutz-Jeghers 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 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 926583	NM_000455.5(STK11):c.81C>T (p.His27=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
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 184843	NM_000455.5(STK11):c.90C>T (p.Asp30=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +2 more	GLikely benign
Select item 492568	NM_000455.5(STK11):c.93C>A (p.Ser31=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +1 more	GLikely benign
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 458076	NM_000455.5(STK11):c.96C>T (p.Thr32=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +1 more	GLikely benign
Select item 135930	NM_000455.5(STK11):c.96C>G (p.Thr32=)	STK11	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 230097	NM_000455.5(STK11):c.108C>T (p.Tyr36=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +1 more	GLikely benign
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)	Peutz-Jeghers syndrome +2 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 +2 more	GUncertain significance
Select item 972241	NM_000455.5(STK11):c.115CGC[1] (p.Arg40del)	STK11 (R40del)	Microsatellite (inframe_deletion)	Hereditary cancer-predisposing syndrome +1 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 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 920205	NM_000455.5(STK11):c.124C>T (p.Arg42Trp)	STK11 (R42W)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing 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 492517	NM_000455.5(STK11):c.129C>G (p.Ala43=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 630947	NM_000455.5(STK11):c.135C>T (p.Leu45=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 920930	NM_000455.5(STK11):c.138C>T (p.Ile46=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2774533	NM_000455.5(STK11):c.139G>C (p.Gly47Arg)	STK11 (G47R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	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 1158028	NM_000455.5(STK11):c.147C>T (p.Tyr49=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
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 922681	NM_000455.5(STK11):c.153G>A (p.Met51Ile)	STK11 (M51I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 492518	NM_000455.5(STK11):c.157G>T (p.Asp53Tyr)	STK11 (D53Y)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 485000	NM_000455.5(STK11):c.160C>T (p.Leu54=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 380605	NM_000455.5(STK11):c.163C>T (p.Leu55=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +3 more	GConflicting classifications of pathogenicity
Select item 492519	NM_000455.5(STK11):c.165G>A (p.Leu55=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 630397	NM_000455.5(STK11):c.174C>T (p.Gly58=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 503650	NM_000455.5(STK11):c.180del (p.Ser59_Tyr60insTer)	STK11	Deletion (nonsense)	Peutz-Jeghers syndrome +2 more	GPathogenic
Select item 237796	NM_000455.5(STK11):c.180C>T (p.Tyr60=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +2 more	GLikely benign
Select item 490162	NM_000455.5(STK11):c.181G>A (p.Gly61Ser)	STK11 (G61S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 492520	NM_000455.5(STK11):c.186G>A (p.Lys62=)	STK11	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 628378	NM_000455.5(STK11):c.195G>C (p.Glu65Asp)	STK11 (E65D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
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 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 860013	NM_000455.5(STK11):c.209A>G (p.Glu70Gly)	STK11 (E70G)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +1 more	GUncertain significance
Select item 527847	NM_000455.5(STK11):c.210G>A (p.Glu70=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +1 more	GLikely benign
Select item 1786562	NM_000455.5(STK11):c.213G>T (p.Thr71=)	STK11	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 237797	NM_000455.5(STK11):c.214C>T (p.Leu72=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 392091	NM_000455.5(STK11):c.216G>T (p.Leu72=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +2 more	GLikely benign
Select item 1332654	NM_000455.5(STK11):c.228C>A (p.Ala76=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 925918	NM_000455.5(STK11):c.228C>T (p.Ala76=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 412546	NM_000455.5(STK11):c.234G>A (p.Lys78=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
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 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 141849	NM_000455.5(STK11):c.241AAG[3] (p.Lys84del)	STK11 (K84del)	Microsatellite (inframe_deletion)	Peutz-Jeghers syndrome +2 more	GUncertain significance
Select item 511160	NM_000455.5(STK11):c.243G>A (p.Lys81=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +2 more	GLikely benign
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 486990	NM_000455.5(STK11):c.249G>A (p.Lys83=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 492521	NM_000455.5(STK11):c.264C>T (p.Ile88=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +1 more	GLikely benign
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 392194	NM_000455.5(STK11):c.267C>T (p.Pro89=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +2 more	GLikely benign
Select item 527845	NM_000455.5(STK11):c.270C>T (p.Asn90=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 184995	NM_000455.5(STK11):c.279C>G (p.Ala93=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +3 more	GLikely benign
Select item 821946	NM_000455.5(STK11):c.288G>A (p.Lys96=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
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

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