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Links from Gene

Items: 1 to 100 of 296

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DCC
(S284C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(S148Y)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
DCC
(E1404Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(G1271R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(R1231G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(Q1197H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(R1124C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
DCC
(R1025G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(I996V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(I981F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(P823L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(I817V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(I760V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(T700I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(Y583C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(R386G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(G1294R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADNP2, ALPK2
+90 more
Copy number loss
not specified
GPathogenic
DCC
(N3S)
Single nucleotide variant
(missense variant)
DCC-related disorder
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
DCC-related disorder
GLikely benign
DCC
(H237Y)
Single nucleotide variant
(missense variant)
DCC-related disorder
GBenign
DCC
Single nucleotide variant
(synonymous variant)
DCC-related disorder
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
DCC-related disorder
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
DCC-related disorder
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
DCC-related disorder
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
DCC-related disorder
GLikely benign
DCC
Single nucleotide variant
(intron variant)
DCC-related disorder
GLikely benign
DCC
(V621M)
Single nucleotide variant
(missense variant)
DCC-related disorder
GLikely benign
DCC
(I759M)
Single nucleotide variant
(missense variant)
DCC-related disorder
GBenign
DCC
Single nucleotide variant
(intron variant)
DCC-related disorder
GLikely benign
DCC
(R773H)
Single nucleotide variant
(missense variant)
DCC-related disorder
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
DCC-related disorder
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
DCC-related disorder
GLikely benign
DCC
(A455V)
Single nucleotide variant
(missense variant)
DCC-related disorder
GLikely benign
DCC
(Q460H)
Single nucleotide variant
(missense variant)
DCC-related disorder
GBenign
DCC
Single nucleotide variant
(synonymous variant)
DCC-related disorder
GLikely benign
DCC
(S1406fs)
Duplication
(frameshift variant)
DCC-related disorder
GUncertain significance
DCC
(P736*)
Indel
(nonsense)
not provided
GPathogenic
DCC
(A1225S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DCC
(Q851*)
Single nucleotide variant
(nonsense)
Mirror movements 1
GLikely pathogenic
DCC
(N533S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DCC
Copy number loss
not provided
GUncertain significance
C18orf54, CCDC68
+8 more
Copy number gain
not provided
GUncertain significance
DCC
(Q1193H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DCC
(V503A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
(T1091S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
(H237N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
Single nucleotide variant
(splice acceptor variant)
not provided
GUncertain significance
DCC
(P1275R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DCC
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DCC
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DCC
(P1150S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DCC
(E512*)
Single nucleotide variant
(nonsense)
DCC-related disorder
GLikely pathogenic
DCC
(R501*)
Single nucleotide variant
(nonsense)
DCC-related disorder
GLikely pathogenic
DCC
Single nucleotide variant
(splice acceptor variant)
DCC-related disorder
GLikely pathogenic
DCC
(I760fs)
Deletion
(frameshift variant)
Mirror movements 1
GPathogenic
DCC
(S194F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(S892R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
Single nucleotide variant
(intron variant)
not specified
GUncertain significance
DCC
(Y1019C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC, MIR4528
Copy number loss
Mirror movements 1
GUncertain significance
DCC
(Q1260*)
Single nucleotide variant
(nonsense)
Mirror movements 1
GLikely pathogenic
DCC
(N555D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(W332R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(I280M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
(P1396S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
(R211P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
(S1169C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
(P423R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
Single nucleotide variant
(splice donor variant)
Mirror movements 1 and/or agenesis of the corpus callosum
GPathogenic
DCC
(A323fs)
Microsatellite
(frameshift variant)
not provided
GPathogenic
DCC
(S412G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(S595I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(E147K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(P847fs)
Deletion
(frameshift variant)
Inborn genetic diseases
GPathogenic
DCC
(P516T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(P622S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(P373S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
(N248S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
(T1067A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DCC
(T146fs)
Microsatellite
(frameshift variant)
not provided
GLikely pathogenic
DCC
(L385*)
Single nucleotide variant
(nonsense)
Mirror movements 1
GPathogenic
DCC
(D206V)
Single nucleotide variant
(missense variant)
Autism spectrum disorder
GLikely pathogenic
DCC
(Y768*)
Single nucleotide variant
(nonsense)
Mirror movements 1
GLikely pathogenic
DCC
(K419fs)
Deletion
(frameshift variant)
Mirror movements 1
GLikely pathogenic
DCC
(S1137G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(G1143S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(P1237T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(N678S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
DCC
(P729A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(G84R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DCC
(G556S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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