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AAACCACCCACCTTCACCATGTCTG[A/T]CGAGGAAGTGTGAGTACCCAGCTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600692 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TNNT3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
TNNT3 - troponin T3, fast skeletal type | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042780.2 | 49 | Missense Mutation | GAC,GTC | D,V 3 | NP_001036245.1 | |
NM_001042781.2 | 49 | Missense Mutation | GAC,GTC | D,V 3 | NP_001036246.1 | |
NM_001042782.2 | 49 | Missense Mutation | GAC,GTC | D,V 3 | NP_001036247.1 | |
NM_001297646.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | NP_001284575.1 | |
NM_006757.3 | 49 | Missense Mutation | GAC,GTC | D,V 3 | NP_006748.1 | |
XM_006718288.3 | 49 | Intron | XP_006718351.1 | |||
XM_006718290.3 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_006718353.1 | |
XM_006718293.2 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_006718356.1 | |
XM_006718294.3 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_006718357.1 | |
XM_006718296.3 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_006718359.1 | |
XM_006718299.2 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_006718362.1 | |
XM_006718300.3 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_006718363.1 | |
XM_006718302.3 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_006718365.1 | |
XM_011520343.2 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_011518645.1 | |
XM_017018205.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873694.1 | |
XM_017018206.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873695.1 | |
XM_017018207.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873696.1 | |
XM_017018208.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873697.1 | |
XM_017018209.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873698.1 | |
XM_017018210.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873699.1 | |
XM_017018211.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873700.1 | |
XM_017018212.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873701.1 | |
XM_017018213.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873702.1 | |
XM_017018214.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873703.1 | |
XM_017018215.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873704.1 | |
XM_017018216.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873705.1 | |
XM_017018217.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873706.1 | |
XM_017018218.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873707.1 | |
XM_017018219.1 | 49 | Missense Mutation | GAC,GTC | D,V 3 | XP_016873708.1 |