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Items: 1 to 100 of 157

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STK11
Deletion
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
Peutz-Jeghers syndrome
GLikely pathogenic
STK11
Deletion
Peutz-Jeghers syndrome
GPathogenic
STK11
Duplication
Peutz-Jeghers syndrome
GLikely pathogenic
STK11
Deletion
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
Peutz-Jeghers syndrome
GPathogenic
STK11
(P321fs)
Indel
(frameshift variant +1 more)
Peutz-Jeghers syndrome
GPathogenic
STK11
(F157fs)
Deletion
(frameshift variant +1 more)
Peutz-Jeghers syndrome
GPathogenic
STK11
(M22fs)
Duplication
(frameshift variant +1 more)
Peutz-Jeghers syndrome
GPathogenic
STK11
Indel
(splice donor variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(A241fs)
Duplication
(frameshift variant +1 more)
Peutz-Jeghers syndrome
GPathogenic
STK11
(T250fs)
Deletion
(frameshift variant +1 more)
Peutz-Jeghers syndrome
GPathogenic
STK11
(S216fs)
Duplication
(frameshift variant +1 more)
Peutz-Jeghers syndrome
GPathogenic
STK11
(M125fs)
Deletion
(frameshift variant +1 more)
Peutz-Jeghers syndrome
GPathogenic
STK11
(Y272*)
Duplication
(nonsense +1 more)
Peutz-Jeghers syndrome
GPathogenic
STK11
(L201fs)
Deletion
(frameshift variant +1 more)
Peutz-Jeghers syndrome
GPathogenic
STK11
Single nucleotide variant
(splice donor variant)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic/Likely pathogenic
STK11
(S271fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Single nucleotide variant
(intron variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(Q152fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Single nucleotide variant
(splice donor variant)
Peutz-Jeghers syndrome
GLikely pathogenic
STK11
(E165fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(K296*)
Single nucleotide variant
(nonsense)
Peutz-Jeghers syndrome
GPathogenic
STK11
Insertion
Peutz-Jeghers syndrome
GPathogenic
STK11
Single nucleotide variant
(splice donor variant)
Peutz-Jeghers syndrome
GLikely pathogenic
STK11
(D53fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
(nonsense +1 more)
Peutz-Jeghers syndrome
GPathogenic
STK11
(M129fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
LOC130062899, STK11
(Q364*)
Single nucleotide variant
(nonsense)
Peutz-Jeghers syndrome
+1 more
GPathogenic
STK11
(Q159*)
Single nucleotide variant
(nonsense)
Peutz-Jeghers syndrome
+1 more
GPathogenic
STK11
(Y292*)
Single nucleotide variant
(nonsense)
not provided
+2 more
GPathogenic
STK11
Deletion
(splice donor variant)
Peutz-Jeghers syndrome
GLikely pathogenic
STK11
(L117fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
Peutz-Jeghers syndrome
GPathogenic
STK11
(L164fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
Peutz-Jeghers syndrome
GPathogenic
STK11
(Q152*)
Single nucleotide variant
(nonsense)
Peutz-Jeghers syndrome
GPathogenic
STK11
(L45fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(V110fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(Q37fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(P144fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(M11fs)
Duplication
(frameshift variant)
Melanoma, cutaneous malignant, susceptibility to, 1
+1 more
GPathogenic/Likely pathogenic
STK11
(L117fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(P314fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(E223fs)
Microsatellite
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Insertion
(nonsense)
Peutz-Jeghers syndrome
GPathogenic
STK11
(Q7*)
Single nucleotide variant
(nonsense)
Peutz-Jeghers syndrome
GPathogenic
STK11
(L195fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Single nucleotide variant
(splice donor variant)
Peutz-Jeghers syndrome
GPathogenic/Likely pathogenic
STK11
(K48fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic/Likely pathogenic
STK11
Single nucleotide variant
(splice donor variant)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic
STK11
(L282fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
Peutz-Jeghers syndrome
GPathogenic
LOC130062899, STK11
(V337fs)
Microsatellite
(frameshift variant)
Peutz-Jeghers syndrome
+1 more
GPathogenic
STK11
(Y49fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(P203fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Duplication
(splice donor variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(Q112*)
Single nucleotide variant
(nonsense)
Peutz-Jeghers syndrome
GPathogenic
STK11
Single nucleotide variant
(splice acceptor variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(I111fs)
Insertion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
Peutz-Jeghers syndrome
GPathogenic
STK11
(Q214fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
(nonsense)
Peutz-Jeghers syndrome
GPathogenic
STK11
(L263*)
Single nucleotide variant
(nonsense)
Peutz-Jeghers syndrome
GPathogenic
STK11
(R297fs)
Microsatellite
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Single nucleotide variant
(splice donor variant)
Peutz-Jeghers syndrome
+1 more
GPathogenic
STK11
Single nucleotide variant
(splice acceptor variant)
Peutz-Jeghers syndrome
GLikely pathogenic
STK11
Single nucleotide variant
(splice donor variant)
Peutz-Jeghers syndrome
+1 more
GPathogenic
STK11
(K312fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(A205fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(K97fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
+1 more
GPathogenic
STK11
(L105*)
Single nucleotide variant
(nonsense)
Peutz-Jeghers syndrome
GPathogenic
STK11
Single nucleotide variant
(splice donor variant)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic/Likely pathogenic
STK11
(Y118*)
Single nucleotide variant
(nonsense)
Peutz-Jeghers syndrome
GPathogenic
STK11
(S232fs)
Microsatellite
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(K97*)
Single nucleotide variant
(nonsense)
Peutz-Jeghers syndrome
GPathogenic
STK11
Single nucleotide variant
(splice acceptor variant)
Peutz-Jeghers syndrome
GUncertain significance
STK11
(E33fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(I88fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Single nucleotide variant
(splice acceptor variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Single nucleotide variant
(splice acceptor variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
Peutz-Jeghers syndrome
GPathogenic
STK11
(D258fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
+1 more
GPathogenic
STK11
(I322fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(Y166*)
Single nucleotide variant
(nonsense)
Peutz-Jeghers syndrome
GPathogenic
STK11
(P324fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
(splice donor variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(F255fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
(splice acceptor variant)
Peutz-Jeghers syndrome
GLikely pathogenic
STK11
(P254fs)
Duplication
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
(V66fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
ABCA7, ARHGAP45
+14 more
Deletion
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
Peutz-Jeghers syndrome
GPathogenic
LOC130062898, LOC110006317
+6 more
Deletion
Peutz-Jeghers syndrome
GPathogenic
STK11
(Y36fs)
Deletion
(frameshift variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Single nucleotide variant
(splice acceptor variant)
Peutz-Jeghers syndrome
GPathogenic
STK11
Deletion
(splice donor variant)
Peutz-Jeghers syndrome
+1 more
GLikely pathogenic
STK11
(N181fs)
Deletion
(frameshift variant)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic
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