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GGTTGAGACACTGTGTGGCTTGGCT[A/G]GTGGGTCTTCTTCCTGCAGACCCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 185861 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SV2B 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
|
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
|
SV2B - synaptic vesicle glycoprotein 2B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167580.1 | Intron | NP_001161052.1 | ||||
NM_001323031.1 | Intron | NP_001309960.1 | ||||
NM_001323032.1 | Intron | NP_001309961.1 | ||||
NM_001323033.1 | Intron | NP_001309962.1 | ||||
NM_001323034.1 | Intron | NP_001309963.1 | ||||
NM_001323036.1 | Intron | NP_001309965.1 | ||||
NM_001323037.1 | Intron | NP_001309966.1 | ||||
NM_001323038.1 | Intron | NP_001309967.1 | ||||
NM_001323039.1 | Intron | NP_001309968.1 | ||||
NM_001323040.1 | Intron | NP_001309969.1 | ||||
NM_014848.5 | Intron | NP_055663.1 | ||||
XM_005254998.3 | Intron | XP_005255055.1 | ||||
XM_017022761.1 | Intron | XP_016878250.1 | ||||
XM_017022762.1 | Intron | XP_016878251.1 |