Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 191041 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
MIR7975 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
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African American - Not Available | YRI (Yoruba) - Not Available | |||||||||
SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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MIR7975 - microRNA 7975 | ||||||
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There are no transcripts associated with this gene. |
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 | 1014 | Silent Mutation | CGG,CGT | R,R 249 | NP_001119604.1 | |
NM_001126133.2 | 1014 | Silent Mutation | CGG,CGT | R,R 238 | NP_001119605.1 | |
NM_001291774.1 | 1014 | Silent Mutation | CGG,CGT | R,R 238 | NP_001278703.1 | |
NM_003283.5 | 1014 | Silent Mutation | CGG,CGT | R,R 265 | NP_003274.3 | |
XM_011527246.2 | 1014 | Silent Mutation | CGG,CGT | R,R 245 | XP_011525548.1 | |
XM_017027186.1 | 1014 | Silent Mutation | CGG,CGT | R,R 249 | XP_016882675.1 | |
XM_017027187.1 | 1014 | Silent Mutation | CGG,CGT | R,R 245 | XP_016882676.1 |
Set Membership: |
HapMap Validated |