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Items: 17

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STK11
(E57fs)
Duplication
(frameshift variant)
not provided
+2 more
GPathogenic/Likely pathogenic
STK11
Single nucleotide variant
(synonymous variant)
Breast and/or ovarian cancer
+4 more
GBenign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(intron variant)
STK11-related condition
+5 more
GBenign/Likely benign
STK11
Single nucleotide variant
(synonymous variant)
STK11-related condition
+4 more
GConflicting classifications of pathogenicity
STK11
(D194N)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic/Likely pathogenic
STK11
Single nucleotide variant
(intron variant)
not provided
+2 more
GBenign
STK11
Single nucleotide variant
(synonymous variant)
Breast and/or ovarian cancer
+4 more
GConflicting classifications of pathogenicity
STK11
(E293*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
STK11
Single nucleotide variant
not provided
+1 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+3 more
GBenign
STK11
Single nucleotide variant
(splice acceptor variant)
not provided
GPathogenic
STK11
Single nucleotide variant
(splice acceptor variant)
not provided
GPathogenic
LOC130062899, STK11
(D330fs)
Duplication
(frameshift variant)
not provided
GPathogenic
LOC130062899, STK11
(F354L)
Single nucleotide variant
(missense variant)
Melanoma, cutaneous malignant, susceptibility to, 1
+7 more
GBenign/Likely benign
LOC130062899, STK11
(E357K)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
STK11
(S404F)
Single nucleotide variant
(missense variant)
STK11-related condition
+5 more
GConflicting classifications of pathogenicity
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