Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAAGAAGGCGGCGGAAGACAGGAGC[A/G]AGCAGGTCTGCGCCTCCCCGGCCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 191010 | ||||||||||||||||||||
Literature Links: |
TPM1 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 |
TPM1 - tropomyosin 1 (alpha) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000366.5 | 743 | Missense Mutation | AAG,GAG | K,E 37 | NP_000357.3 | |
NM_001018004.1 | 743 | Missense Mutation | AAG,GAG | K,E 37 | NP_001018004.1 | |
NM_001018005.1 | 743 | Missense Mutation | AAG,GAG | K,E 37 | NP_001018005.1 | |
NM_001018006.1 | 743 | Missense Mutation | AAG,GAG | K,E 37 | NP_001018006.1 | |
NM_001018007.1 | 743 | Missense Mutation | AAG,GAG | K,E 37 | NP_001018007.1 | |
NM_001018008.1 | 743 | Intron | NP_001018008.1 | |||
NM_001018020.1 | 743 | Missense Mutation | AAG,GAG | K,E 37 | NP_001018020.1 | |
NM_001301244.1 | 743 | Missense Mutation | AAG,GAG | K,E 37 | NP_001288173.1 | |
NM_001301289.1 | 743 | Intron | NP_001288218.1 | |||
XM_005254637.1 | 743 | Missense Mutation | AAG,GAG | K,E 37 | XP_005254694.1 | |
XM_005254638.3 | 743 | Missense Mutation | AAG,GAG | K,E 121 | XP_005254695.2 | |
XM_005254639.3 | 743 | Missense Mutation | AAG,GAG | K,E 121 | XP_005254696.2 | |
XM_005254645.2 | 743 | Missense Mutation | AAG,GAG | K,E 121 | XP_005254702.2 | |
XM_005254646.2 | 743 | Intron | XP_005254703.1 | |||
XM_005254647.3 | 743 | Intron | XP_005254704.1 | |||
XM_005254650.3 | 743 | Intron | XP_005254707.1 | |||
XM_005254651.1 | 743 | Intron | XP_005254708.1 | |||
XM_005254652.1 | 743 | Intron | XP_005254709.1 | |||
XM_005254653.2 | 743 | Intron | XP_005254710.1 | |||
XM_006720667.3 | 743 | Missense Mutation | AAG,GAG | K,E 121 | XP_006720730.2 | |
XM_017022534.1 | 743 | Missense Mutation | AAG,GAG | K,E 121 | XP_016878023.1 | |
XM_017022535.1 | 743 | Missense Mutation | AAG,GAG | K,E 37 | XP_016878024.1 | |
XM_017022536.1 | 743 | Missense Mutation | AAG,GAG | K,E 121 | XP_016878025.1 | |
XM_017022537.1 | 743 | Missense Mutation | AAG,GAG | K,E 37 | XP_016878026.1 | |
XM_017022538.1 | 743 | Missense Mutation | AAG,GAG | K,E 121 | XP_016878027.1 | |
XM_017022539.1 | 743 | Missense Mutation | AAG,GAG | K,E 121 | XP_016878028.1 | |
XM_017022540.1 | 743 | Intron | XP_016878029.1 | |||
XM_017022541.1 | 743 | Intron | XP_016878030.1 |