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TCTCCTCTCACCCACTAAATACAGC[C/T]GGAGGGCTTATGGCTTATTCTGTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609677 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
OS9 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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OS9 - OS9, endoplasmic reticulum lectin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001017956.2 | Intron | NP_001017956.1 | ||||
NM_001017957.2 | Intron | NP_001017957.1 | ||||
NM_001017958.2 | Intron | NP_001017958.1 | ||||
NM_001261420.1 | Intron | NP_001248349.1 | ||||
NM_001261421.1 | Intron | NP_001248350.1 | ||||
NM_001261422.1 | Intron | NP_001248351.1 | ||||
NM_001261423.1 | Intron | NP_001248352.1 | ||||
NM_006812.3 | Intron | NP_006803.1 | ||||
XM_005268581.1 | Intron | XP_005268638.1 | ||||
XM_006719200.1 | Intron | XP_006719263.1 | ||||
XM_006719201.1 | Intron | XP_006719264.1 |