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CCTTGAAACACAAAACAACAGATGC[A/G]CCACCTTACATTAAAACAGCCCTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609619 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GOLGA8B 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
|
GOLGA8B - golgin A8 family member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001023567.4 | Intron | NP_001018861.3 | ||||
XM_011521596.1 | Intron | XP_011519898.1 | ||||
XM_011521597.1 | Intron | XP_011519899.1 | ||||
XM_017022210.1 | Intron | XP_016877699.1 | ||||
XM_017022211.1 | Intron | XP_016877700.1 | ||||
XM_017022212.1 | Intron | XP_016877701.1 | ||||
XM_017022213.1 | Intron | XP_016877702.1 | ||||
XM_017022214.1 | Intron | XP_016877703.1 | ||||
XM_017022215.1 | Intron | XP_016877704.1 | ||||
XM_017022216.1 | Intron | XP_016877705.1 | ||||
XM_017022217.1 | Intron | XP_016877706.1 | ||||
XM_017022218.1 | Intron | XP_016877707.1 |