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GCACGTACTTGACGCGGATGGACAC[A/G]TCGGTGTTGCGCGTGTTGTAGAAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607162 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ST8SIA5 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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ST8SIA5 - ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001307986.1 | 1537 | Silent Mutation | NP_001294915.1 | |||
NM_001307987.1 | 1537 | Silent Mutation | NP_001294916.1 | |||
NM_013305.5 | 1537 | Silent Mutation | NP_037437.2 | |||
XM_017025715.1 | 1537 | Silent Mutation | XP_016881204.1 | |||
XM_017025716.1 | 1537 | Silent Mutation | XP_016881205.1 |