U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from Gene

Items: 1 to 100 of 259

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DOCK1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DOCK1, INSYN2A
(L111F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(R288W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(L127F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(K112R)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
DOCK1, INSYN2A
(V256I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(R160Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1
(T22M +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1
(S1692L +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(V1824L +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(P188S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1
(A266T +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(R1490C +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(D1162E +8 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(G1349S +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ABRAXAS2, ACADSB
+80 more
Copy number loss
not provided
GPathogenic
DOCK1, INSYN2A
(S319N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(S301L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(R290G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(R288Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
DOCK1, INSYN2A
(E287Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(A276T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(A25S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(G233E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(R232Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(L225I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(D221Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(D221N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(S217P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(R214Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(G205A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(P199L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(T183I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(A164V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(N140D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(R122H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(V105M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(V99I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(R85H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(A82T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(G472R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(D357N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(I349T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, INSYN2A
(V340A)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
DOCK1, LOC126861085
(S291L +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, LOC126861085
(R292M +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, LOC126861085
(K260E +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1
(Y231H +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1
(S1818L +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(A1724V +12 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
DOCK1
(P1700S +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(D1631G +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(S1387F +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(V1668I +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(S1476G +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(R1379Q +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(R1240Q +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1
(V118G +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1
(K1128R +8 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(R116Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1
(V959I +8 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(E705G +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(S617F +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1, LOC105378552
(V464M +7 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
DOCK1, LOC105378552
(K475E +6 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DOCK1, LOC105378552
(Y378C +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1, LOC105378552
(R141G +5 more)
Single nucleotide variant
(non-coding transcript variant +2 more)
not specified
GUncertain significance
DOCK1
(N347S +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ABRAXAS2, ADAM12
+55 more
Copy number loss
not specified
GPathogenic
DOCK1, INSYN2A
Copy number loss
not specified
GUncertain significance
DOCK1, FOXI2
+2 more
Copy number loss
not specified
GUncertain significance
ABCC2, ABLIM1
+293 more
Copy number gain
not specified
GPathogenic
ABRAXAS2, ADAM12
+54 more
Copy number loss
not specified
GPathogenic
DOCK1
Copy number loss
not specified
GUncertain significance
LOC126861083, LOC126861084
+201 more
Copy number loss
Duane syndrome type 1
+1 more
GPathogenic
DOCK1
(R1016* +8 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
DOCK1, INSYN2A
Copy number loss
not provided
GUncertain significance
ADAM8, ADGRA1
+38 more
Copy number loss
not provided
GPathogenic
DOCK1
Copy number loss
not provided
GUncertain significance
ABLIM1, ABRAXAS2
+117 more
Copy number gain
not provided
GPathogenic
DOCK1
(K1430R +12 more)
Single nucleotide variant
(missense variant)
EBV-positive nodal T- and NK-cell lymphoma
GLikely benign
ABLIM1, ABRAXAS2
+145 more
Copy number gain
Distal trisomy 10q
GPathogenic
TCERG1L, TCERG1L-AS1
+38 more
Copy number loss
Distal 10q deletion syndrome
GPathogenic
DOCK1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DOCK1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DOCK1, LOC105378552
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
DOCK1
(M856I +8 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(R1590L +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(K1420N +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(R1526K +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(M1036T +8 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(T649P +8 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(V1146I +8 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(Q852H +8 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(R1826C +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1
(M739I +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DOCK1, LOC105378552
(V453I +7 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ABRAXAS2, ADAM12
+62 more
Copy number loss
Distal 10q deletion syndrome
GPathogenic
AGAP5, CRTAC1
+682 more
Copy number gain
Distal trisomy 10q
GPathogenic
GLRX3, GPR26
+77 more
Copy number loss
Distal 10q deletion syndrome
GPathogenic
Format
Items per page
Sort by
Choose Destination