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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNT1
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
TNNT1
Single nucleotide variant
(intron variant)
not provided
GBenign
TNNT1
Single nucleotide variant
(intron variant)
not provided
GBenign
TNNT1
Single nucleotide variant
(intron variant)
not provided
GBenign
TNNT1
(E180* +1 more)
Single nucleotide variant
(nonsense)
Nemaline myopathy 5
GPathogenic
TNNT1
Single nucleotide variant
(synonymous variant)
Nemaline myopathy 5
+1 more
GConflicting classifications of pathogenicity
TNNT1
Single nucleotide variant
(intron variant)
not provided
GBenign
TNNT1
Single nucleotide variant
(intron variant)
not provided
GBenign
TNNT1
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign/Likely benign
TNNI3, TNNT1
(E12G)
Single nucleotide variant
(missense variant)
Nemaline myopathy 5
+5 more
GBenign/Likely benign
TNNT1
Single nucleotide variant
(intron variant)
not provided
GBenign
TNNT1, TNNI3
Single nucleotide variant
(5 prime UTR variant)
Dilated Cardiomyopathy, Recessive
+6 more
GBenign/Likely benign
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