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Items: 1 to 100 of 130

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129933244, LOC129933245
+653 more
Copy number gain
See cases
GPathogenic
LOC126806103, LOC126806104
+1047 more
Copy number gain
See cases
GPathogenic
ACP1, ADAM17
+498 more
Copy number gain
See cases
GPathogenic
LOC129933186, LOC129933187
+736 more
Copy number gain
See cases
GPathogenic
ABHD1, ACP1
+893 more
Copy number gain
See cases
GPathogenic
LOC129933311, LOC129933312
+1631 more
Copy number gain
See cases
GPathogenic
LINC01115, LINC01121
+1400 more
Copy number gain
See cases
GPathogenic
ADAM17, ADI1
+546 more
Copy number gain
See cases
GPathogenic
HAAO, HADHA
+2457 more
Copy number gain
See cases
GBenign
APOB, APOB-ICR
+131 more
Copy number loss
See cases
GPathogenic
RAD51AP2
(M1141T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(H1135Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(L1134F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(R1130K +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RAD51AP2
(R1122K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(I1121V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(R1110T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(R1110G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(R1082S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(Y1077H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(R1061S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(P1045S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(P1029L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(R1017H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(M1010T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(E1007D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(F969C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(F959C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(D952Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(E923K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(N919D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(I918V +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RAD51AP2
(Y895C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(N875I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(M867V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(F856S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(D844A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(K825E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(Y820N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(S822G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(L806V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(I773L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(S766G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(V756I +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RAD51AP2
(I733M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(H716D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(W723R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(N713D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(N719I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(M711V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(N701S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(Q709R +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RAD51AP2
(S701P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(E690K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(D693Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(I679N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(T674I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(L657V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(R650G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(P636R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(K610E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(P609S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(V572I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(S571N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(T548A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(Q548K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(I545T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(H508R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(N485S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(T466R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(T466M +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RAD51AP2
(V454I +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RAD51AP2
(E448D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(I429L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(K425N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(M414K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(R404K +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RAD51AP2
(V390F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(V376I +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RAD51AP2
(K365R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(S354P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(S338G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(S347R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(D344G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(D344N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(I313V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(P251L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(I257V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(D244E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(D244Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(K233N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(P219L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(A205V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(A205T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
RAD51AP2
(T192I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(D185H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(L184V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(S147N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAD51AP2
(V155F +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
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