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- SNP ID:
- rs78619110
- Gene
-
ST6GAL2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.2: 106811930 - 106811930 on Build GRCh38
- Polymorphism:
- G/A, Transition substitution
- Context Sequence [VIC/FAM]:
TAAAAAGTCCAGGGGAACCAGGTGC[G/A]AGCTTCAAGAATCCACTCCCAGGGA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608472
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Literature Links: |
ST6GAL2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
| ST6GAL2 - ST6 beta-galactoside alpha-2,6-sialyltransferase 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001142351.1 | 2999 | Intron | NP_001135823.1 | |||
| NM_001142352.1 | 2999 | Intron | NP_001135824.1 | |||
| NM_001322362.1 | 2999 | Intron | NP_001309291.1 | |||
| NM_032528.2 | 2999 | Intron | NP_115917.1 | |||
| XM_006712802.1 | 2999 | Intron | XP_006712865.1 | |||
| XM_011511999.2 | 2999 | Intron | XP_011510301.1 | |||
| XM_011512000.2 | 2999 | Intron | XP_011510302.1 | |||
| XM_011512001.2 | 2999 | UTR 3 | XP_011510303.1 | |||
| XM_017005110.1 | 2999 | Intron | XP_016860599.1 | |||
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