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Items: 33

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VCAN
(S300L)
Single nucleotide variant
(missense variant)
Wagner syndrome
+3 more
GBenign
VCAN
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GConflicting classifications of pathogenicity
VCAN
Single nucleotide variant
(intron variant +1 more)
not provided
GConflicting classifications of pathogenicity
VCAN
(S569R)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
VCAN
(W622R)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GBenign/Likely benign
VCAN
(T632M)
Single nucleotide variant
(intron variant +1 more)
Wagner syndrome
+3 more
GBenign/Likely benign
VCAN
(G723E)
Single nucleotide variant
(intron variant +1 more)
not provided
GUncertain significance
VCAN
(M836V)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
VCAN
(A892T)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
VCAN
(W983*)
Single nucleotide variant
(intron variant +1 more)
not provided
GUncertain significance
VCAN
(R1238T)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+4 more
GConflicting classifications of pathogenicity
VCAN
(H1319Q)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
VCAN, VCAN-AS1
Single nucleotide variant
(synonymous variant +1 more)
not specified
+3 more
GBenign
VCAN, VCAN-AS1
(K1516E +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+4 more
GConflicting classifications of pathogenicity
VCAN-AS1, VCAN
(K1516R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GBenign
VCAN, VCAN-AS1
(E1535G +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GBenign/Likely benign
VCAN, VCAN-AS1
Single nucleotide variant
(synonymous variant +1 more)
not specified
+3 more
GBenign/Likely benign
VCAN, VCAN-AS1
(R1826H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GBenign
VCAN, VCAN-AS1
Single nucleotide variant
(synonymous variant +1 more)
not specified
+3 more
GBenign
VCAN, VCAN-AS1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
VCAN, VCAN-AS1
Single nucleotide variant
(synonymous variant +1 more)
Vitreoretinopathy
+3 more
GBenign
VCAN, VCAN-AS1
(L2256P +1 more)
Single nucleotide variant
(missense variant +1 more)
VCAN-related condition
+3 more
GConflicting classifications of pathogenicity
VCAN, VCAN-AS1
(T2282A +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
VCAN, VCAN-AS1
(F2301C +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
VCAN, VCAN-AS1
(F2301Y +1 more)
Single nucleotide variant
(missense variant +1 more)
Wagner syndrome
+3 more
GBenign
VCAN, VCAN-AS1
(G2312R +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
VCAN-AS1, VCAN
Single nucleotide variant
(synonymous variant +1 more)
VCAN-related condition
+1 more
GConflicting classifications of pathogenicity
VCAN, VCAN-AS1
(A2874V +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GConflicting classifications of pathogenicity
VCAN, VCAN-AS1
Single nucleotide variant
(synonymous variant +1 more)
not specified
+3 more
GBenign/Likely benign
VCAN, VCAN-AS1
(D2937Y +1 more)
Single nucleotide variant
(missense variant +1 more)
Wagner syndrome
+3 more
GBenign
VCAN, VCAN-AS1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GUncertain significance
VCAN, VCAN-AS1
(A3035V +1 more)
Single nucleotide variant
(missense variant +1 more)
Wagner syndrome
+3 more
GBenign
VCAN-AS1, VCAN
(L3152V +3 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
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