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Links from Gene

Items: 1 to 100 of 120

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UNC5B
(S773I +1 more)
Single nucleotide variant
(missense variant)
UNC5B-related disorder
GUncertain significance
UNC5B
(R798S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(P530L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(S345C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R544T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R68G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(S24T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(P330A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(A304V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(G281R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(D207N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(L188V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R175H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(Q109H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(V928M +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
UNC5B
(L876F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(H754R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(H759R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(E730G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(K714R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(V688I +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
UNC5B
(R683Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(E627K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R605H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(N558S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(Q522H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(V471I +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
UNC5B
(Q449R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R442C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(D409Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(G372E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(D396N +1 more)
Single nucleotide variant
(missense variant)
UNC5B-related disorder
GLikely benign
UNC5B
(V371M +1 more)
Single nucleotide variant
(missense variant)
UNC5B-related disorder
GLikely benign
UNC5B
(R852H +1 more)
Single nucleotide variant
(missense variant)
UNC5B-related disorder
GLikely benign
CDH23, SLC29A3
+1 more
Copy number gain
not provided
GUncertain significance
RRP12, RTKN2
+332 more
Copy number gain
not provided
GPathogenic
UNC5B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
UNC5B
(V728M +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
UNC5B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
UNC5B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
UNC5B
(L779F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(P412R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(L97P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(A818V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(G736R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(I455N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGAP5, CRTAC1
+682 more
Copy number gain
Distal trisomy 10q
GPathogenic
ABRAXAS2, CHCHD1
+673 more
Copy number loss
Distal 10q deletion syndrome
GPathogenic
UNC5B
(R264Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R142C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(L492P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(A418T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(G943R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(Y78H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(D407A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R322C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R106H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(L535W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(E830K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R813Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(T293N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R106C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(C130G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R175L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(V146I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(A382V +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
UNC5B
(R802W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R8P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(L693F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R324H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R721Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(I230F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R721W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R514C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R605C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R678H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(P434L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(Q820H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(T683M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(Q94R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(T341M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(V847A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(L103R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(A449T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(L67H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(G553S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R114Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R234H)
Single nucleotide variant
(missense variant)
Autism spectrum disorder
+1 more
GConflicting classifications of pathogenicity
UNC5B
(E111D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(S460A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(T446R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(W19R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(T827A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(N201S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(K268N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(R555K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(D529Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(P762R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(M935T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UNC5B
(V386M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
Display optionsSort by RelevanceDownload
Format
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