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CAAACACAACTTATAAATACCCCAA[C/T]CCCTTTTAATATTCCTGGCTTGCCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610950 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SYT16 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SYT16 - synaptotagmin 16 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_031914.2 | Intron | NP_114120.2 | ||||
XM_006720272.3 | Intron | XP_006720335.1 | ||||
XM_011537219.1 | Intron | XP_011535521.1 | ||||
XM_011537220.1 | Intron | XP_011535522.1 | ||||
XM_011537221.2 | Intron | XP_011535523.1 | ||||
XM_011537222.2 | Intron | XP_011535524.1 | ||||
XM_011537223.2 | Intron | XP_011535525.1 | ||||
XM_011537224.2 | Intron | XP_011535526.1 | ||||
XM_011537225.2 | Intron | XP_011535527.1 | ||||
XM_011537227.2 | Intron | XP_011535529.2 | ||||
XM_011537228.2 | Intron | XP_011535530.1 | ||||
XM_011537229.2 | Intron | XP_011535531.1 | ||||
XM_017021693.1 | Intron | XP_016877182.1 | ||||
XM_017021694.1 | Intron | XP_016877183.1 | ||||
XM_017021695.1 | Intron | XP_016877184.1 | ||||
XM_017021696.1 | Intron | XP_016877185.1 | ||||
XM_017021697.1 | Intron | XP_016877186.1 | ||||
XM_017021698.1 | Intron | XP_016877187.1 |