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GTCATTATTTGTGATACCTGGGTAT[C/G]AGAGGCATGGCAGGAAAATATCAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
11 submissions
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Phenotype: |
MIM: 610949 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SYT14 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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SYT14 - synaptotagmin 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146261.2 | Intron | NP_001139733.1 | ||||
NM_001146262.2 | Intron | NP_001139734.1 | ||||
NM_001146264.2 | Intron | NP_001139736.1 | ||||
NM_001256006.1 | Intron | NP_001242935.1 | ||||
NM_153262.3 | Intron | NP_694994.2 | ||||
XM_006711262.3 | Intron | XP_006711325.1 | ||||
XM_017000931.1 | Intron | XP_016856420.1 | ||||
XM_017000932.1 | Intron | XP_016856421.1 | ||||
XM_017000933.1 | Intron | XP_016856422.1 | ||||
XM_017000934.1 | Intron | XP_016856423.1 | ||||
XM_017000935.1 | Intron | XP_016856424.1 |