U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 66

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABHD8, ACP5
+2135 more
Copy number gain
See cases
GPathogenic
ABHD8, ADGRE2
+695 more
Copy number gain
See cases
GPathogenic
ABHD8, AKAP8
+574 more
Copy number gain
See cases
GPathogenic
LOC130064154, LOC130064155
+625 more
Copy number gain
See cases
GPathogenic
SUGP1
(P640R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(R631C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(S613A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(I606M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(K556R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(K542R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(A475E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(W472L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(M457T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
SUGP1
(P428A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(P428T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SUGP1
(S411P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(Q403R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(P397A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(K393E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(A376T)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SUGP1
(P370S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(P361R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(P361S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(A355S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(P339S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(R336C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(G333R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(G325V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(F316I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(R310Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(S303N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(Q287R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(E261K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(D260N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(A245V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(K243R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(K243E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(E240G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(M211L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(E201K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(F198S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(K179R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
SUGP1
(Q162R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(V154L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(G133A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(T132I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(I128L)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SUGP1
(A121T)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SUGP1
(A109V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(Q97E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(I79F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(S77F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(E69K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(Q58H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
(A40T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SUGP1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
SUGP1
(M5V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC6, ATP13A1
+36 more
Copy number loss
not specified
GUncertain significance
BORCS8, HAPLN4
+9 more
Copy number gain
not provided
GUncertain significance
BST2, NWD1
+158 more
Copy number gain
not provided
GPathogenic
BORCS8, HAPLN4
+8 more
Copy number gain
not provided
GUncertain significance
PGLYRP1, PGLYRP2
+1364 more
Copy number gain
See cases
GPathogenic
TMC4, TMED1
+1364 more
Copy number gain
See cases
GPathogenic
ATP13A1, BORCS8
+49 more
Complex
Breast ductal adenocarcinoma
GUncertain significance
Format
Items per page
Sort by
Choose Destination