Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGTTGAGCCCTGTGGTAGGCACAG[A/G]TGCACCCGACCAGCACCTGGAGCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
30 submissions
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Phenotype: |
MIM: 605632 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC35A3 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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SLC35A3 - solute carrier family 35 member A3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271684.1 | 125 | Intron | NP_001258613.1 | |||
NM_001271685.1 | 125 | Missense Mutation | GAT,GGT | D,G 14 | NP_001258614.1 | |
NM_012243.2 | 125 | Intron | NP_036375.1 | |||
XM_005270691.4 | 125 | Intron | XP_005270748.1 | |||
XM_011541135.2 | 125 | Missense Mutation | GAT,GGT | D,G 14 | XP_011539437.1 | |
XM_011541136.2 | 125 | UTR 5 | XP_011539438.1 | |||
XM_011541137.2 | 125 | Missense Mutation | GAT,GGT | D,G 14 | XP_011539439.1 | |
XM_011541138.2 | 125 | Missense Mutation | GAT,GGT | D,G 14 | XP_011539440.1 | |
XM_017000869.1 | 125 | Intron | XP_016856358.1 | |||
XM_017000870.1 | 125 | Intron | XP_016856359.1 | |||
XM_017000871.1 | 125 | Intron | XP_016856360.1 | |||
XM_017000872.1 | 125 | Intron | XP_016856361.1 |
Set Membership: |
HapMap |