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ATTAGCCTCTGACTGTTTGCTCAGC[G/T]GCTCTTCAGTGAAAGTGATATAGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
6 submissions
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Phenotype: |
MIM: 610804 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC35D1 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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SLC35D1 - solute carrier family 35 member D1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015139.2 | 1472 | Missense Mutation | CAG,CCG | Q,P 336 | NP_055954.1 | |
XM_006710478.1 | 1472 | Missense Mutation | CAG,CCG | Q,P 363 | XP_006710541.1 | |
XM_011541070.1 | 1472 | Missense Mutation | CAG,CCG | Q,P 363 | XP_011539372.1 |