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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TCAP
Single nucleotide variant
(synonymous variant)
Primary familial hypertrophic cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
TCAP
(S64L)
Single nucleotide variant
(missense variant)
Primary familial hypertrophic cardiomyopathy
+6 more
GBenign
TCAP
(R70W)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2G
+5 more
GUncertain significance
TCAP
(R106C)
Single nucleotide variant
(missense variant)
not provided
+7 more
GBenign/Likely benign
TCAP
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+4 more
GBenign
TCAP
Single nucleotide variant
(3 prime UTR variant)
Autosomal recessive limb-girdle muscular dystrophy type 2G
+2 more
GConflicting classifications of pathogenicity
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