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Items: 1 to 100 of 211

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130004500, LOC130004501
+821 more
Copy number gain
See cases
GPathogenic
EDRF1-AS1, EDRF1-DT
+1036 more
Copy number gain
See cases
GPathogenic
GSTO1, GSTO2
+1097 more
Copy number gain
See cases
GPathogenic
LOC124416905, LOC124416906
+318 more
Copy number loss
See cases
GPathogenic
ABLIM1, ACSL5
+308 more
Copy number loss
See cases
GPathogenic
LOC126861107, LOC128598885
+802 more
Copy number gain
See cases
GPathogenic
ADD3, ADD3-AS1
+28 more
Copy number gain
See cases
GUncertain significance
ADD3
(S3L)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
ADD3
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ADD3
(S6I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADD3
(Q7H)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ADD3
(G8S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ADD3
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ADD3
(V9M)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ADD3
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ADD3
(Y24D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADD3
(R27C)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
ADD3
(N29S +2 more)
Single nucleotide variant
(missense variant +1 more)
Cerebral palsy, spastic quadriplegic, 3
GPathogenic
ADD3
(N29S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ADD3
(M41V)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ADD3
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ADD3
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ADD3
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ADD3
(R57Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADD3
(Q63H)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
ADD3
(S64I)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ADD3
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ADD3
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ADD3
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ADD3
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ADD3
(G82D +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
ADD3
(T8A +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ADD3
(I16M +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADD3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADD3
(S102P +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign/Likely benign
ADD3
(S104L +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
ADD3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADD3
(G105S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(L111F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
Deletion
(intron variant)
not provided
GBenign
ADD3
(G114C +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ADD3
(D126G +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(T127A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADD3
(L58F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(T137I +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ADD3
(R138L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(C139Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADD3
(C139S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(K140I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADD3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADD3
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ADD3
Duplication
(intron variant)
not provided
GBenign
ADD3
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ADD3
Single nucleotide variant
(synonymous variant)
not provided
GBenign/Likely benign
ADD3
(K167R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(D92Y +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(I94F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(G100D +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADD3
(T107A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(K113T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(V198M +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(S125N +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADD3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADD3
(G134E +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(F135V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(S136G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADD3
(I141V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(T222A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADD3
Single nucleotide variant
(intron variant)
not provided
GBenign
ADD3
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
ADD3
(V162A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADD3
(S164F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADD3
(D181V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADD3
(D259G +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ADD3
(A261S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADD3
(D186V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(P206R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADD3
(S207N +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(E305G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADD3
(N312D +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ADD3
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ADD3
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ADD3
(N254S +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ADD3
(H334R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADD3
(K264E +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
ADD3
(A272V +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ADD3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ADD3
(G354R +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
ADD3
(G355V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(S282A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADD3
(G367D +1 more)
Single nucleotide variant
(missense variant)
Cerebral palsy, spastic quadriplegic, 3
GPathogenic/Likely pathogenic
ADD3
(T299I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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