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GGTACTTGGGATGGAAAAATAGAAC[C/G]TTTTGTCTTGCTTTAGACTCTTCGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610139 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ST8SIA6 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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ST8SIA6 - ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001004470.1 | 877 | Missense Mutation | AAC,AAG | N,K 295 | NP_001004470.1 | |
XM_017016174.1 | 877 | Missense Mutation | AAC,AAG | N,K 265 | XP_016871663.1 | |
XM_017016175.1 | 877 | Intron | XP_016871664.1 |