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Items: 1 to 100 of 190

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TPM1
Single nucleotide variant
(5 prime UTR variant +1 more)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(5 prime UTR variant)
Cardiomyopathy
+1 more
GUncertain significance
TPM1
Single nucleotide variant
(5 prime UTR variant +1 more)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(5 prime UTR variant +1 more)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(5 prime UTR variant +1 more)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(5 prime UTR variant)
Dilated cardiomyopathy 1Y
+2 more
GUncertain significance
TPM1
(M10fs)
Duplication
(frameshift variant)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Y
+6 more
GConflicting classifications of pathogenicity
TPM1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GLikely benign
TPM1
(K12*)
Single nucleotide variant
(nonsense)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+1 more
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign/Likely benign
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
+1 more
GLikely benign
TPM1
(R21L)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+7 more
GConflicting classifications of pathogenicity
TPM1
(A22G)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+1 more
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+1 more
GLikely benign
TPM1
(A27T)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
GUncertain significance
TPM1
(D28H)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 21
+5 more
GUncertain significance
TPM1
(D28N)
Single nucleotide variant
(missense variant)
not specified
+4 more
GUncertain significance
TPM1
(A32S)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
TPM1
(A32V)
Single nucleotide variant
(missense variant +1 more)
Hypertrophic cardiomyopathy
+1 more
GUncertain significance
TPM1
(D34N)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
GLikely benign
TPM1
(R35K)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
TPM1
(R35S)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
TPM1
(Q38E)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+1 more
GUncertain significance
TPM1
Single nucleotide variant
(intron variant)
Cardiomyopathy
+4 more
GUncertain significance
TPM1
Single nucleotide variant
(intron variant)
Cardiomyopathy
+1 more
GUncertain significance
TPM1
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign/Likely benign
TPM1
Single nucleotide variant
(intron variant)
Cardiomyopathy
GLikely benign
TPM1
Single nucleotide variant
(intron variant)
Cardiomyopathy
+1 more
GConflicting classifications of pathogenicity
TPM1
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
TPM1
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GBenign
TPM1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+3 more
GBenign/Likely benign
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
GLikely benign
TPM1
(E54V)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
TPM1
(E56D)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
GLikely benign
TPM1
(R57Q)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
+2 more
GBenign/Likely benign
TPM1
(R59W)
Single nucleotide variant
(missense variant +1 more)
Primary familial hypertrophic cardiomyopathy
+1 more
GConflicting classifications of pathogenicity
TPM1
Single nucleotide variant
(intron variant +1 more)
not provided
+1 more
GLikely benign
TPM1
(S70N)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
+2 more
GBenign/Likely benign
TPM1
(E76del)
Indel
(inframe_deletion +1 more)
Cardiomyopathy
GLikely benign
TPM1
(E75fs)
Indel
(frameshift variant +1 more)
Cardiomyopathy
GLikely benign
TPM1
Single nucleotide variant
(intron variant)
Cardiomyopathy
GLikely benign
TPM1
Single nucleotide variant
(intron variant)
Cardiomyopathy
GLikely benign
TPM1
(E40* +1 more)
Single nucleotide variant
(nonsense +1 more)
Cardiomyopathy
+6 more
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
+1 more
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
+1 more
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
+2 more
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
+1 more
GLikely benign
TPM1
(K93T +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
GUncertain significance
TPM1
(G52S +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
TPM1
(D55G +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
+2 more
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
+3 more
GBenign/Likely benign
TPM1
Single nucleotide variant
(synonymous variant +1 more)
not specified
+3 more
GBenign/Likely benign
TPM1
(S61C +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
+1 more
GUncertain significance
TPM1
(E62G +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
GUncertain significance
TPM1
(D108H +1 more)
Single nucleotide variant
(missense variant +1 more)
Hypertrophic cardiomyopathy
+2 more
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
+1 more
GLikely benign
TPM1
(E111D +1 more)
Single nucleotide variant
(intron variant +2 more)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
GLikely benign
LOC130057222, TPM1
+1 more
(D22G)
Single nucleotide variant
(non-coding transcript variant +2 more)
Cardiomyopathy
GLikely benign
LOC130057222, TPM1
+1 more
(L41P)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
GLikely benign
TPM1
Single nucleotide variant
(intron variant)
Cardiomyopathy
+1 more
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+4 more
GConflicting classifications of pathogenicity
TPM1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+3 more
GLikely benign
TPM1
(D84E +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+4 more
GUncertain significance
TPM1
(V85I +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GLikely benign
TPM1
(R55C +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GUncertain significance
TPM1
(R55H +2 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy
+2 more
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy
+2 more
GLikely benign
TPM1
(R101G +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
+1 more
GLikely benign
TPM1
(R105H +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+3 more
GUncertain significance
TPM1
(A107P +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy
+1 more
GLikely benign
TPM1
Single nucleotide variant
(intron variant)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(intron variant)
Cardiomyopathy
+4 more
GBenign/Likely benign
TPM1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Y
+5 more
GConflicting classifications of pathogenicity
TPM1
(I130T +2 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+4 more
GConflicting classifications of pathogenicity
TPM1
(K100N +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy
+2 more
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy
+7 more
GBenign/Likely benign
TPM1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Y
+4 more
GConflicting classifications of pathogenicity
TPM1
Single nucleotide variant
(synonymous variant)
not provided
+6 more
GBenign/Likely benign
TPM1
Single nucleotide variant
(intron variant)
Cardiomyopathy
+1 more
GLikely benign
TPM1
Single nucleotide variant
(intron variant)
not specified
+4 more
GConflicting classifications of pathogenicity
TPM1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+1 more
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Y
+6 more
GConflicting classifications of pathogenicity
TPM1
(D175N +2 more)
Single nucleotide variant
(missense variant)
not provided
+6 more
GPathogenic
TPM1
(A183V +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
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