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Search Thermo Fisher Scientific
GGCATGGCGCAGGGCGGCCACCTCG[C/T]GGGCCATGCGCTCCCGCCCGAAGGC
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
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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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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 | 1160 | Missense Mutation | CAC,CGC | H,R 329 | NP_001305032.1 | |
NM_001318104.1 | 1160 | Missense Mutation | CAC,CGC | H,R 329 | NP_001305033.1 | |
NM_001318105.1 | 1160 | Missense Mutation | CAC,CGC | H,R 329 | NP_001305034.1 | |
NM_001318106.1 | 1160 | Missense Mutation | CAC,CGC | H,R 329 | NP_001305035.1 | |
NM_001318107.1 | 1160 | Missense Mutation | CAC,CGC | H,R 330 | NP_001305036.1 | |
NM_001318108.1 | 1160 | Missense Mutation | CAC,CGC | H,R 329 | NP_001305037.1 | |
NM_001318109.1 | 1160 | Missense Mutation | CAC,CGC | H,R 354 | NP_001305038.1 | |
NM_001318110.1 | 1160 | Missense Mutation | CAC,CGC | H,R 329 | NP_001305039.1 | |
NM_001318111.1 | 1160 | Missense Mutation | CAC,CGC | H,R 329 | NP_001305040.1 | |
NM_001318112.1 | 1160 | Missense Mutation | CAC,CGC | H,R 329 | NP_001305041.1 | |
NM_001318113.1 | 1160 | Missense Mutation | CAC,CGC | H,R 329 | NP_001305042.1 | |
NM_001318114.1 | 1160 | Missense Mutation | CAC,CGC | H,R 330 | NP_001305043.1 | |
NM_001318115.1 | 1160 | Missense Mutation | CAC,CGC | H,R 329 | NP_001305044.1 | |
NM_001318116.1 | 1160 | Missense Mutation | CAC,CGC | H,R 329 | NP_001305045.1 | |
NM_004861.2 | 1160 | Missense Mutation | CAC,CGC | H,R 329 | NP_004852.1 | |
XM_011530518.2 | 1160 | Missense Mutation | CAC,CGC | H,R 356 | XP_011528820.1 | |
XM_011530522.2 | 1160 | Missense Mutation | CAC,CGC | H,R 330 | XP_011528824.1 | |
XM_011530524.1 | 1160 | Missense Mutation | CAC,CGC | H,R 330 | XP_011528826.1 | |
XM_011530528.1 | 1160 | Missense Mutation | CAC,CGC | H,R 330 | XP_011528830.1 | |
XM_017029096.1 | 1160 | Missense Mutation | CAC,CGC | H,R 330 | XP_016884585.1 | |
XM_017029097.1 | 1160 | Missense Mutation | CAC,CGC | H,R 330 | XP_016884586.1 | |
XM_017029098.1 | 1160 | Missense Mutation | CAC,CGC | H,R 329 | XP_016884587.1 |
SEC14L6 - SEC14 like lipid binding 6 | ||||||
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There are no transcripts associated with this gene. |