Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCTCCCCCATGTAGTCAATGTCCA[G/T]AGGCTTCTTACGCTCGGAGAGGATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 191041 | ||||||||||||||||||||
Literature Links: |
TNNT1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
TNNT1 - troponin T1, slow skeletal type | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001126132.2 | 844 | Missense Mutation | ATG,CTG | M,L 193 | NP_001119604.1 | |
NM_001126133.2 | 844 | Missense Mutation | ATG,CTG | M,L 182 | NP_001119605.1 | |
NM_001291774.1 | 844 | Missense Mutation | ATG,CTG | M,L 182 | NP_001278703.1 | |
NM_003283.5 | 844 | Missense Mutation | ATG,CTG | M,L 193 | NP_003274.3 | |
XM_011527246.2 | 844 | Missense Mutation | ATG,CTG | M,L 189 | XP_011525548.1 | |
XM_017027186.1 | 844 | Missense Mutation | ATG,CTG | M,L 193 | XP_016882675.1 | |
XM_017027187.1 | 844 | Missense Mutation | ATG,CTG | M,L 189 | XP_016882676.1 |