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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VCL
(T197I)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
VCL
Single nucleotide variant
(intron variant)
not provided
+3 more
GBenign
VCL
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
VCL
(I519L)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+6 more
GConflicting classifications of pathogenicity
VCL
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
VCL
(P796L)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+1 more
GUncertain significance
VCL
(L818Q)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
VCL
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GConflicting classifications of pathogenicity
VCL
(A934V)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+4 more
GBenign/Likely benign
VCL
(L955del)
Deletion
(inframe_deletion +1 more)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
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