U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 52

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
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
(E16Q)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GConflicting classifications of pathogenicity
TPM1
(R21L)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+7 more
GConflicting classifications of pathogenicity
TPM1
(A22T)
Single nucleotide variant
(missense variant)
not specified
+5 more
GConflicting classifications of pathogenicity
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
(K30del)
Microsatellite
(inframe_deletion)
TPM1-related disorder
+1 more
GLikely pathogenic
TPM1
(R35S)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
TPM1
(S36R)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
GUncertain significance
TPM1
(S36G)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 3
+3 more
GUncertain significance
TPM1
Single nucleotide variant
(intron variant)
Cardiomyopathy
+1 more
GUncertain significance
TPM1
Single nucleotide variant
(intron variant)
Cardiomyopathy
GUncertain significance
TPM1
(D55G +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
+2 more
GUncertain significance
TPM1
(D108H +1 more)
Single nucleotide variant
(missense variant +1 more)
Hypertrophic cardiomyopathy
+2 more
GUncertain significance
TPM1
(E72K +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
+1 more
GUncertain significance
TPM1
Single nucleotide variant
(intron variant)
Cardiomyopathy
+1 more
GLikely benign
TPM1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+3 more
GLikely benign
TPM1
(L88V +2 more)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Y
+3 more
GUncertain significance
TPM1
(R55H +2 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GUncertain significance
TPM1
(A102T +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GLikely benign
TPM1
(E115K +2 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
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
(Q144R +2 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+2 more
GUncertain significance
TPM1
(I154V +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+3 more
GConflicting classifications of pathogenicity
TPM1
Single nucleotide variant
(synonymous variant)
not provided
+6 more
GBenign/Likely 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
TPM1
(E187V +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+2 more
GConflicting classifications of pathogenicity
TPM1
Single nucleotide variant
(intron variant)
not specified
+1 more
GConflicting classifications of pathogenicity
TPM1
(E192K +2 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+5 more
GPathogenic/Likely pathogenic
TPM1
(E212V +2 more)
Single nucleotide variant
(missense variant +1 more)
Hypertrophic cardiomyopathy 1
+2 more
GUncertain significance
TPM1
(S215L +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GPathogenic/Likely pathogenic
TPM1
(I225V +2 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
GLikely benign
TPM1
(E207K +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
TPM1
(R244K +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GUncertain significance
TPM1
(L249W +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
+1 more
GConflicting classifications of pathogenicity
TPM1
(K266R +1 more)
Single nucleotide variant
(intron variant +1 more)
Cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
TPM1
Single nucleotide variant
(synonymous variant +1 more)
Cardiovascular phenotype
+2 more
GLikely benign
TPM1
(D244N +1 more)
Single nucleotide variant
(missense variant +1 more)
Hypertrophic cardiomyopathy
+1 more
GUncertain significance
TPM1
(M281T +1 more)
Single nucleotide variant
(intron variant +1 more)
not provided
+5 more
GPathogenic/Likely pathogenic
TPM1
(I284V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+5 more
GConflicting classifications of pathogenicity
TPM1
Single nucleotide variant
(3 prime UTR variant +1 more)
Hypertrophic cardiomyopathy
+1 more
GConflicting classifications of pathogenicity
TPM1
Single nucleotide variant
(3 prime UTR variant +1 more)
Cardiomyopathy
GUncertain significance
TPM1
Single nucleotide variant
(3 prime UTR variant +1 more)
Left ventricular noncompaction cardiomyopathy
+3 more
GConflicting classifications of pathogenicity
TPM1
(L261fs +1 more)
Deletion
(3 prime UTR variant +2 more)
not specified
+1 more
GUncertain significance
Format
Items per page
Sort by
Choose Destination