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Items: 1 to 100 of 2394

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STK11
Translocation
Adrenal cortex carcinoma
GUncertain significance
STK11
Single nucleotide variant
not provided
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Duplication
(splice donor variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Deletion
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GBenign
STK11
Single nucleotide variant
(5 prime UTR variant)
not provided
+1 more
GBenign
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GBenign
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
+1 more
GBenign/Likely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
not provided
+1 more
GBenign/Likely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GBenign
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GBenign/Likely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
+1 more
GBenign/Likely benign
STK11
Duplication
(5 prime UTR variant)
Peutz-Jeghers syndrome
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Deletion
(5 prime UTR variant)
not specified
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
not specified
GBenign
STK11
Single nucleotide variant
(5 prime UTR variant)
not provided
GBenign
STK11
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GLikely benign
STK11
Deletion
(5 prime UTR variant)
Peutz-Jeghers syndrome
+1 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
not specified
+2 more
GLikely benign
STK11
Duplication
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
not specified
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
not specified
+2 more
GConflicting classifications of pathogenicity
STK11
Deletion
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
STK11
Duplication
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
+4 more
GConflicting classifications of pathogenicity
STK11
(M1V)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
STK11
(M1L)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
STK11
(E2Q)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
STK11
(E2G)
Single nucleotide variant
(missense variant +1 more)
Peutz-Jeghers syndrome
GUncertain significance
STK11
(E2A)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+3 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
(V4del)
Microsatellite
(inframe_deletion)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
STK11
(V3L)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
STK11
(V3M)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
STK11
(V3G)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
(V4L)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
(V4L)
Single nucleotide variant
(missense variant)
Melanoma, cutaneous malignant, susceptibility to, 1
+1 more
GUncertain significance
STK11
(V4M)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
STK11
(V4G)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
STK11
(V4A)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GLikely benign
STK11
(D5N)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
(D5G)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
STK11
(P6S)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
(P6T)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
(P6L)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
(P6R)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
GLikely benign
STK11
(Q7K)
Indel
(missense variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
(Q7*)
Single nucleotide variant
(nonsense)
Peutz-Jeghers syndrome
GPathogenic
STK11
(Q7R)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
(Q8K)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
(Q8E)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
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