Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGGCCCCCGTCGATGCAGATGGTC[C/T]GCATGCGCTCGTTGGCATGGCGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602300 | ||||||||||||||||||||
Literature Links: |
GAL3ST1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
GAL3ST1 - galactose-3-O-sulfotransferase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318103.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 342 | NP_001305032.1 | |
NM_001318104.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 342 | NP_001305033.1 | |
NM_001318105.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 342 | NP_001305034.1 | |
NM_001318106.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 342 | NP_001305035.1 | |
NM_001318107.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 343 | NP_001305036.1 | |
NM_001318108.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 342 | NP_001305037.1 | |
NM_001318109.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 367 | NP_001305038.1 | |
NM_001318110.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 342 | NP_001305039.1 | |
NM_001318111.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 342 | NP_001305040.1 | |
NM_001318112.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 342 | NP_001305041.1 | |
NM_001318113.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 342 | NP_001305042.1 | |
NM_001318114.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 343 | NP_001305043.1 | |
NM_001318115.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 342 | NP_001305044.1 | |
NM_001318116.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 342 | NP_001305045.1 | |
NM_004861.2 | 1199 | Missense Mutation | CAG,CGG | Q,R 342 | NP_004852.1 | |
XM_011530518.2 | 1199 | Missense Mutation | CAG,CGG | Q,R 369 | XP_011528820.1 | |
XM_011530522.2 | 1199 | Missense Mutation | CAG,CGG | Q,R 343 | XP_011528824.1 | |
XM_011530524.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 343 | XP_011528826.1 | |
XM_011530528.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 343 | XP_011528830.1 | |
XM_017029096.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 343 | XP_016884585.1 | |
XM_017029097.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 343 | XP_016884586.1 | |
XM_017029098.1 | 1199 | Missense Mutation | CAG,CGG | Q,R 342 | XP_016884587.1 |
SEC14L6 - SEC14 like lipid binding 6 | ||||||
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There are no transcripts associated with this gene. |