"Clinical Genetics, Academic Medical Center"[submitter] AND "STK11"[ge - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 93097	NM_000455.5(STK11):c.264C>A (p.Ile88=)	STK11	Single nucleotide variant (synonymous variant)	not specified +4 more	GBenign
Select item 139332	NM_000455.5(STK11):c.465-18G>T	STK11	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 182881	NM_000455.5(STK11):c.597+14del	STK11	Deletion (intron variant)	Peutz-Jeghers syndrome +4 more	GBenign/Likely benign
Select item 135924	NM_000455.5(STK11):c.598-8C>T	STK11	Single nucleotide variant (intron variant)	not specified +6 more	GBenign/Likely benign
Select item 215740	NM_000455.5(STK11):c.598-7G>A	STK11	Single nucleotide variant (intron variant)	STK11-related condition +5 more	GBenign/Likely benign
Select item 139335	NM_000455.5(STK11):c.787T>C (p.Leu263=)	STK11	Single nucleotide variant (synonymous variant)	Breast and/or ovarian cancer +5 more	GBenign/Likely benign
Select item 141192	NM_000455.5(STK11):c.816C>T (p.Tyr272=)	STK11	Single nucleotide variant (synonymous variant)	not specified +4 more	GBenign
Select item 93099	NM_000455.5(STK11):c.920+7G>C	STK11	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign
Select item 135929	NM_000455.5(STK11):c.945G>A (p.Pro315=)	STK11	Single nucleotide variant (synonymous variant)	Breast and/or ovarian cancer +5 more	GBenign/Likely benign
Select item 7461	NM_000455.5(STK11):c.1062C>G (p.Phe354Leu)	LOC130062899, STK11 (F354L)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +7 more	GBenign/Likely benign
Select item 135915	NM_000455.5(STK11):c.1185A>G (p.Thr395=)	STK11	Single nucleotide variant (synonymous variant)	Breast and/or ovarian cancer +4 more	GConflicting classifications of pathogenicity
Select item 184516	NM_000455.5(STK11):c.1200G>A (p.Leu400=)	STK11	Single nucleotide variant (synonymous variant)	Peutz-Jeghers syndrome +4 more	GBenign/Likely benign
Select item 127700	NM_000455.5(STK11):c.1211C>T (p.Ser404Phe)	STK11 (S404F)	Single nucleotide variant (missense variant)	STK11-related condition +5 more	GConflicting classifications of pathogenicity
Select item 139339	NM_000455.5(STK11):c.1296G>A (p.Gln432=)	STK11	Single nucleotide variant (synonymous variant)	Breast and/or ovarian cancer +4 more	GConflicting classifications of pathogenicity