Product Details

SNP ID
rs45576635
Assay Type
Functionally tested
NCBI dbSNP Submissions
17
Location
Chr.1:201359577 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGGGATAGCTGGAAGGTAGGGAAG[A/G]AGGGGGCAGGGGGAGGGCTAGGCGA
Phenotype
MIM: 191045
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TNNT2 PubMed Links

Gene Details

Gene
TNNT2
Gene Name
troponin T2, cardiac type
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000364.3 Intron NP_000355.2
NM_001001430.2 Intron NP_001001430.1
NM_001001431.2 Intron NP_001001431.1
NM_001001432.2 Intron NP_001001432.1
NM_001276345.1 Intron NP_001263274.1
NM_001276346.1 Intron NP_001263275.1
NM_001276347.1 Intron NP_001263276.1
XM_006711508.3 Intron XP_006711571.1
XM_006711509.3 Intron XP_006711572.1
XM_011509938.2 Intron XP_011508240.1
XM_011509939.1 Intron XP_011508241.1
XM_011509940.2 Intron XP_011508242.1
XM_011509941.2 Intron XP_011508243.1
XM_011509942.2 Intron XP_011508244.1
XM_011509943.2 Intron XP_011508245.1
XM_011509944.2 Intron XP_011508246.1
XM_011509946.1 Intron XP_011508248.1
XM_017002216.1 Intron XP_016857705.1
XM_017002217.1 Intron XP_016857706.1

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