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Items: 1 to 100 of 695

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STK11
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GLikely benign
STK11
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+2 more
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
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing 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 provided
+4 more
GConflicting classifications of pathogenicity
STK11
(M1L)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
STK11
(E2A)
Single nucleotide variant
(missense variant)
Melanoma, cutaneous malignant, susceptibility to, 1
+3 more
GUncertain significance
STK11
(V4del)
Microsatellite
(inframe_deletion)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
STK11
(V3L)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
(V3M)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+2 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
STK11
(P6L)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
STK11
(P6R)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
(Q8E)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
(L9V)
Single nucleotide variant
(missense variant)
Germ cell tumor of testis
+5 more
GUncertain significance
STK11
(L9Q)
Single nucleotide variant
(missense variant)
Melanoma, cutaneous malignant, susceptibility to, 1
+2 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+1 more
GLikely benign
STK11
(M11L)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+3 more
GUncertain significance
STK11
(M11V)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+3 more
GUncertain significance
STK11
Deletion
(inframe_indel)
Hereditary cancer-predisposing syndrome
GUncertain significance
STK11
(M11I)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
(T13M)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
STK11
(E14G)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
STK11
(E14D)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+3 more
GBenign/Likely benign
STK11
(G15S)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+2 more
GLikely benign
STK11
(L17V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
STK11
(M18I)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
STK11
(S19L)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign/Likely benign
STK11
(G21S)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
STK11
(T24R)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
STK11
(T24M)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GBenign/Likely benign
STK11
(D30E)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
(T32A)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign/Likely benign
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+1 more
GLikely benign
STK11
(Q37R)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
(P38A)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
STK11
(P38L)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+2 more
GUncertain significance
STK11
(R40del)
Microsatellite
(inframe_deletion)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
(R39C)
Single nucleotide variant
(missense variant)
Melanoma, cutaneous malignant, susceptibility to, 1
+2 more
GUncertain significance
STK11
(R39L)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
STK11
(R42W)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
(R42L)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
STK11
(R42Q)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
STK11
(A43V)
Single nucleotide variant
(missense variant)
Melanoma, cutaneous malignant, susceptibility to, 1
+2 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+2 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+1 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
(G47R)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
STK11
(K48R)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+2 more
GLikely benign
STK11
(M51L)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
STK11
(M51I)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
(D53Y)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
STK11
Deletion
(nonsense)
Peutz-Jeghers syndrome
+2 more
GPathogenic
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+2 more
GLikely benign
STK11
(G61S)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+2 more
GLikely benign
STK11
(E65D)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
STK11
(V66M)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
STK11
(S69L)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
STK11
(E70G)
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
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+2 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+3 more
GBenign/Likely benign
STK11
(K81Q)
Single nucleotide variant
(missense variant)
Peutz-Jeghers syndrome
+1 more
GUncertain significance
STK11
(K84del)
Microsatellite
(inframe_deletion)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
STK11
(K83R)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+1 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+4 more
GBenign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Peutz-Jeghers syndrome
+3 more
GLikely benign
STK11
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
STK11
Microsatellite
(splice donor variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
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