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Links from Gene

Items: 1 to 100 of 135

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CASP8AP2
(D173N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(A1518D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(V636F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(V1517A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(V603A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(H987R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(P1416T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(P573T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(K1749E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(H1086R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(D917V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(S743C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(H1612Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(N893D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(S1746N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BACH2, CASP8AP2
+3 more
Deletion
not provided
GUncertain significance
CASP8AP2
(Y291C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(G28A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(R257T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(D1890A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(R1784S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(K1775E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(V1705A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(V1623F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(N1526H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(D1480V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(S1334N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(I1244V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(E1216G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(Y1205H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(K1148E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(R1118H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(K999E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(R957S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(P892L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(P877S)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CASP8AP2
(T811I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(V792D)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CASP8AP2
(D735N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(V716I)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CASP8AP2
(M598V)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CASP8AP2
(S597L)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CASP8AP2
(K512R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(A453V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(V451A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ANKRD6, BACH2
+4 more
Copy number gain
not specified
GUncertain significance
AKIRIN2, ANKRD6
+24 more
Copy number loss
not provided
GPathogenic
CASP8AP2
(A618V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(G271D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(V1623L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(R229L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(N782D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(V790I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(H1476Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(T326N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(H332Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(N7S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(I1233M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(S253N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(I648V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(R707K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(M1668R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(K1147R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(A19G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(Q1720H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(R1836T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(P766R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(E952G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(I1708V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(S1183R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(Y73H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(M668V)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CASP8AP2
(R964W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(A1884V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(K1284R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(T1282P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(T1019N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(P573R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(K1688R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(K1339T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(N1681S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(V1209L)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CASP8AP2
(V1425I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(S1507G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(K552T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(K1213R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(D1307E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(T898A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(I1103V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(E656K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(C1587F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(S1868F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(C1713Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(T986S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(S1018N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(V1684I)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CASP8AP2
(R972C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(L1829W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(I1239V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CASP8AP2
(E1104G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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