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Links from Gene

Items: 1 to 100 of 130

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LATS2
(P297R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(T931M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(A470S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(R590K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(G268R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(L523P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(G498R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(N1029Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYL1, EEF1AKMT1
+16 more
Deletion
not provided
GPathogenic
CDX2, AMER2
+82 more
Copy number gain
not provided
GUncertain significance
LATS2
(P307S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(G250C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(Q249H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P247S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(G193S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(L186M)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
LATS2
(Q148K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(Q1084H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P1033S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P1010S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(M997V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(S979F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(N847H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(N821K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(Q74E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P68S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(G547V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P469S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2, MRPL57
+2 more
Copy number gain
not provided
GUncertain significance
LATS2, XPO4
Copy number gain
not provided
GUncertain significance
LATS2
(R255Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(S91L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(R448L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P514S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(R849W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(C537R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(R849Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(V394L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(R887H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(R1054Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(G310R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P479L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(G385S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P519S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P314Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(A468E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P916S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(G310E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(Y214C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(E24D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(S1074C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(A768T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P256L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(G299S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P221S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(D341N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P38S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(V219A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(V990I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(R558L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LATS2
(P398L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CRYL1, EEF1AKMT1
+18 more
Copy number loss
not provided
GPathogenic
CRYL1, EEF1AKMT1
+19 more
Copy number gain
not provided
GUncertain significance
B3GLCT, HS6ST3
+332 more
Copy number gain
not provided
GPathogenic
ABCC4, ABHD13
+332 more
Copy number gain
Complete trisomy 13 syndrome
GPathogenic
ABCC4, ABHD13
+332 more
Copy number gain
not specified
GPathogenic
VPS36, VWA8
+329 more
Copy number gain
not specified
GPathogenic
ABCC4, ABHD13
+332 more
Copy number gain
not provided
GPathogenic
LATS2, XPO4
Copy number gain
not provided
GUncertain significance
DACH1, IRS2
+332 more
Copy number gain
See cases
GPathogenic
CENPJ, CHAMP1
+332 more
Copy number gain
See cases
GPathogenic
FGF9, LATS2
+5 more
Copy number gain
not provided
GUncertain significance
LATS2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
SKA3, MRPL57
+2 more
Copy number gain
not provided
GLikely benign
LATS2, MRPL57
+2 more
Copy number gain
not provided
GLikely benign
GJB6, IL17D
+13 more
Copy number loss
not provided
GPathogenic
MPHOSPH8, FGF9
+27 more
Copy number loss
not provided
GPathogenic
LATS2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LATS2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LATS2
Single nucleotide variant
(intron variant)
not provided
GBenign
LATS2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LATS2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LATS2
Microsatellite
(inframe_insertion)
not provided
GBenign
LATS2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LATS2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LATS2
(N930S)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
LATS2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LATS2
Single nucleotide variant
(synonymous variant)
not provided
GBenign/Likely benign
LATS2
(D852E)
Single nucleotide variant
(missense variant)
not provided
GBenign
LATS2
(D1013N)
Single nucleotide variant
(missense variant)
not provided
GBenign
LATS2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LATS2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LATS2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LATS2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LATS2
(G563R)
Single nucleotide variant
(missense variant)
not provided
GBenign
ABCC4, ABHD13
+332 more
Copy number gain
not provided
GPathogenic
AMER2, ATP12A
+40 more
Copy number gain
not provided
GPathogenic
CRYL1, EEF1AKMT1
+14 more
Copy number loss
not provided
GPathogenic
CRYL1, EEF1AKMT1
+19 more
Copy number loss
not provided
GPathogenic
CRYL1, EEF1AKMT1
+19 more
Copy number loss
not provided
GLikely pathogenic
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