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- SNP ID:
- rs11826523
- Gene
-
SYT8TNNI2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.11: 1833216 - 1833216 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
GCGCTCCGCCAGCCACGTGTGGGAC[A/G]CCGGACCCACCTGGGAGTGTCCCCC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 607719
MIM: 191043
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Literature Links: |
SYT8 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
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
|
| SYT8 - synaptotagmin 8 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001290332.1 | Intron | NP_001277261.1 | ||||
| NM_001290333.1 | Intron | NP_001277262.1 | ||||
| NM_001290334.1 | Intron | NP_001277263.1 | ||||
| NM_138567.4 | Intron | NP_612634.3 | ||||
| XM_011520455.1 | Intron | XP_011518757.1 | ||||
| XM_011520456.2 | Intron | XP_011518758.1 | ||||
| XM_011520457.2 | Intron | XP_011518759.1 | ||||
| XM_017018528.1 | Intron | XP_016874017.1 | ||||
| XM_017018529.1 | Intron | XP_016874018.1 | ||||
| TNNI2 - troponin I2, fast skeletal type | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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