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Items: 52

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STK11
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+4 more
GConflicting classifications of pathogenicity
STK11
(P38A)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+4 more
GBenign
STK11
(Q100R)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+4 more
GUncertain significance
STK11
(R104S)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GConflicting classifications of pathogenicity
STK11
(N119D)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+2 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GBenign/Likely benign
STK11
Single nucleotide variant
(synonymous variant)
Breast and/or ovarian cancer
+4 more
GBenign/Likely benign
STK11
(R147H)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+3 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(intron variant)
Peutz-Jeghers syndrome
+4 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(intron variant)
not specified
+5 more
GBenign/Likely benign
STK11
Single nucleotide variant
(intron variant)
Breast and/or ovarian cancer
+8 more
GBenign/Likely benign
STK11
Single nucleotide variant
(intron variant)
Breast and/or ovarian cancer
+2 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(intron variant)
not specified
+4 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(intron variant)
not specified
+5 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+2 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
Duplication
(intron variant)
Breast and/or ovarian cancer
+4 more
GBenign/Likely benign
STK11
Deletion
(intron variant)
Breast and/or ovarian cancer
+4 more
GBenign/Likely benign
STK11
Single nucleotide variant
(intron variant)
STK11-related disorder
+5 more
GBenign/Likely benign
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+4 more
GConflicting classifications of pathogenicity
STK11
(R211Q)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GBenign/Likely benign
STK11
(A241T)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+4 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Breast and/or ovarian cancer
+4 more
GBenign/Likely benign
STK11
Single nucleotide variant
(intron variant)
STK11-related disorder
+4 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+3 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+5 more
GBenign/Likely benign
STK11
Single nucleotide variant
(synonymous variant)
Breast and/or ovarian cancer
+4 more
GBenign/Likely benign
STK11
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GBenign
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+4 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+4 more
GBenign/Likely benign
STK11
(P315L)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(synonymous variant)
Breast and/or ovarian cancer
+5 more
GBenign/Likely benign
LOC130062899, STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer
+6 more
GConflicting classifications of pathogenicity
LOC130062899, STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+5 more
GLikely benign
LOC130062899, STK11
(E349A)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
LOC130062899, STK11
(F354L)
Single nucleotide variant
(missense variant)
Melanoma, cutaneous malignant, susceptibility to, 1
+7 more
GBenign/Likely benign
LOC130062899, STK11
Single nucleotide variant
(intron variant)
not provided
+4 more
GConflicting classifications of pathogenicity
STK11
(E376A)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(synonymous variant)
Breast and/or ovarian cancer
+4 more
GConflicting classifications of pathogenicity
STK11
(A397S)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
STK11
(A397V)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
STK11
(S404F)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+5 more
GConflicting classifications of pathogenicity
STK11
(A417S)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+2 more
GConflicting classifications of pathogenicity
STK11
(C418S)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+3 more
GUncertain significance
STK11
(S428L)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(synonymous variant)
Breast and/or ovarian cancer
+4 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+4 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
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