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CTGTAAAGTAACTCGTAGTTGGCTG[A/G]TAAAACTTTGTAAAGCAAGGATCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
15 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) - 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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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 | Intron | NP_001258613.1 | ||||
NM_001271685.1 | Intron | NP_001258614.1 | ||||
NM_012243.2 | Intron | NP_036375.1 | ||||
XM_005270691.4 | Intron | XP_005270748.1 | ||||
XM_011541135.2 | Intron | XP_011539437.1 | ||||
XM_011541136.2 | Intron | XP_011539438.1 | ||||
XM_011541137.2 | Intron | XP_011539439.1 | ||||
XM_011541138.2 | Intron | XP_011539440.1 | ||||
XM_017000869.1 | Intron | XP_016856358.1 | ||||
XM_017000870.1 | Intron | XP_016856359.1 | ||||
XM_017000871.1 | Intron | XP_016856360.1 | ||||
XM_017000872.1 | Intron | XP_016856361.1 |