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TTTCTAGAATCTCTGGTCTGCTGCT[A/G]TGCAGATGGACCTGCCGGCACTGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SYT17 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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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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SYT17 - synaptotagmin 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308157.1 | 482 | Silent Mutation | CTA,CTG | L,L 18 | NP_001295086.1 | |
NM_016524.3 | 482 | Silent Mutation | CTA,CTG | L,L 22 | NP_057608.2 | |
XM_005255362.3 | 482 | UTR 5 | XP_005255419.1 | |||
XM_011545865.1 | 482 | Silent Mutation | CTA,CTG | L,L 38 | XP_011544167.1 | |
XM_011545866.2 | 482 | Silent Mutation | CTA,CTG | L,L 29 | XP_011544168.1 | |
XM_011545868.1 | 482 | Silent Mutation | CTA,CTG | L,L 16 | XP_011544170.1 | |
XM_011545869.2 | 482 | UTR 5 | XP_011544171.1 | |||
XM_011545870.2 | 482 | UTR 5 | XP_011544172.1 | |||
XM_011545871.2 | 482 | UTR 5 | XP_011544173.1 | |||
XM_011545872.2 | 482 | UTR 5 | XP_011544174.1 | |||
XM_017023280.1 | 482 | Silent Mutation | CTA,CTG | L,L 22 | XP_016878769.1 | |
XM_017023281.1 | 482 | UTR 5 | XP_016878770.1 |