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CCGCCTGCTGCCCTGGTGCCGTGGA[C/T]TTCCCCAGCTTGCGCCTGGACCTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605881 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC35C1 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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SLC35C1 - solute carrier family 35 member C1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145265.1 | 1021 | Silent Mutation | GAC,GAT | D,D 90 | NP_001138737.1 | |
NM_001145266.1 | 1021 | Silent Mutation | GAC,GAT | D,D 90 | NP_001138738.1 | |
NM_018389.4 | 1021 | Silent Mutation | GAC,GAT | D,D 103 | NP_060859.4 | |
XM_011520202.2 | 1021 | Intron | XP_011518504.1 | |||
XM_011520203.2 | 1021 | Silent Mutation | GAC,GAT | D,D 103 | XP_011518505.1 |