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Items: 66

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDCP1
(P831A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(S817N)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CDCP1
(A783S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(R782G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(R763Q)
Single nucleotide variant
(missense variant)
not provided
GBenign
CDCP1
(G752S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(R726Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(G725E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(K724R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(K724*)
Single nucleotide variant
(nonsense)
Myoepithelial tumor
GUncertain significance
CDCP1
(K720N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(G705D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(I671T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(L670V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(I669V)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CDCP1
(S635G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(E623K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(I618L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(R612W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(V597M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(G596S)
Single nucleotide variant
(missense variant)
not provided
GBenign
CDCP1
(R594Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(Q584H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(D583N)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CDCP1
(F541L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(A521G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(F520L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(T519N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(H472Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(A464G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(P363T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(E360K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(R353Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(Y345F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(Y345H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(G324W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
CDCP1
(G303R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(E293K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(N270S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(V256I)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CDCP1
(G231A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(A212V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(G208S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(R185Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(V171M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(R166Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(G165S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(S154G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(R145H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(G136S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(Q110H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(T66A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(S61F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(T50I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(I44V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(L23R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1
(V8A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CDCP1, CLEC3B
+12 more
Copy number gain
not provided
GUncertain significance
NCKIPSD, NDUFAF3
+71 more
Copy number loss
not provided
GPathogenic
CDCP1, CLEC3B
+16 more
Copy number loss
not provided
GUncertain significance
APEH, HEMK1
+177 more
Copy number gain
not provided
GPathogenic
ABHD5, ACAA1
+135 more
Copy number gain
not provided
GPathogenic
HHLA2, HIGD1A
+1054 more
Copy number gain
See cases
GPathogenic
A4GNT, AADAC
+1054 more
Copy number gain
See cases
GPathogenic
ABHD5, ACAA1
+177 more
Copy number gain
See cases
GLikely pathogenic
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