Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGGTACGCCCCGAGGGTGCAGGCTG[C/T]GTCGTAGTACAGCTCGTGGTAGTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608472 | ||||||||||||||||||||
Literature Links: |
ST6GAL2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ST6GAL2 - ST6 beta-galactoside alpha-2,6-sialyltransferase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142351.1 | 1542 | Missense Mutation | ACA,GCA | T,A 475 | NP_001135823.1 | |
NM_001142352.1 | 1542 | Intron | NP_001135824.1 | |||
NM_001322362.1 | 1542 | Missense Mutation | ACA,GCA | T,A 475 | NP_001309291.1 | |
NM_032528.2 | 1542 | Missense Mutation | ACA,GCA | T,A 475 | NP_115917.1 | |
XM_006712802.1 | 1542 | Missense Mutation | ACA,GCA | T,A 475 | XP_006712865.1 | |
XM_011511999.2 | 1542 | Missense Mutation | ACA,GCA | T,A 475 | XP_011510301.1 | |
XM_011512000.2 | 1542 | Intron | XP_011510302.1 | |||
XM_011512001.2 | 1542 | Intron | XP_011510303.1 | |||
XM_017005110.1 | 1542 | Intron | XP_016860599.1 |