C0031269[trait identifier] AND "KCCC/NGS Laboratory, Kuwait Cancer Con - ClinVar - NCBI

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Items: 19

	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)	Breast and/or ovarian cancer +4 more	GBenign
Select item 256203	NM_000455.5(STK11):c.290+36G>T	STK11	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign
Select item 256204	NM_000455.5(STK11):c.374+24G>T	STK11	Single nucleotide variant	Hereditary cancer-predisposing syndrome +3 more	GBenign
Select item 139331	NM_000455.5(STK11):c.464+9G>A	STK11	Single nucleotide variant (intron variant)	STK11-related condition +5 more	GBenign/Likely benign
Select item 142410	NM_000455.5(STK11):c.464+10C>T	STK11	Single nucleotide variant (intron variant)	STK11-related condition +8 more	GBenign/Likely benign
Select item 142399	NM_000455.5(STK11):c.464+11G>A	STK11	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 412534	NM_000455.5(STK11):c.558C>T (p.Thr186=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +6 more	GBenign/Likely benign
Select item 381849	NM_000455.5(STK11):c.579C>A (p.Ser193=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 492549	NM_000455.5(STK11):c.666C>G (p.Pro222=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 183713	NM_000455.5(STK11):c.666C>T (p.Pro222=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign/Likely benign
Select item 379077	NM_000455.5(STK11):c.734+17C>G	STK11	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 139335	NM_000455.5(STK11):c.787T>C (p.Leu263=)	STK11	Single nucleotide variant (synonymous variant)	STK11-related condition +5 more	GBenign/Likely benign
Select item 182885	NM_000455.5(STK11):c.795G>A (p.Glu265=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign/Likely benign
Select item 141192	NM_000455.5(STK11):c.816C>T (p.Tyr272=)	STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign
Select item 378678	NM_000455.5(STK11):c.863-14C>T	STK11	Single nucleotide variant (intron variant)	Peutz-Jeghers syndrome +2 more	GLikely benign
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)	STK11-related condition +5 more	GBenign/Likely benign
Select item 458010	NM_000455.5(STK11):c.1029C>T (p.Asp343=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 183994	NM_000455.5(STK11):c.1035C>T (p.His345=)	LOC130062899, STK11	Single nucleotide variant (synonymous variant)	STK11-related condition +3 more	GBenign/Likely benign