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TAGGTAGCAAAGAGGCCCTGGGACC[A/G]GGGCTCGGGGGTGGTGGGTAAGGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
9 submissions
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Phenotype: |
MIM: 191045 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TNNT2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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TNNT2 - troponin T2, cardiac type | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | 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 |