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CTATCACTCCGCTGTAAGTGGTTTG[A/G]CCAGCCCGGGCAGCCACCTGTAATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603859 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC25A13 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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SLC25A13 - solute carrier family 25 member 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001160210.1 | 1742 | Silent Mutation | GGC,GGT | G,G 556 | NP_001153682.1 | |
NM_014251.2 | 1742 | Silent Mutation | GGC,GGT | G,G 555 | NP_055066.1 | |
XM_006715831.3 | 1742 | Silent Mutation | GGC,GGT | G,G 566 | XP_006715894.1 | |
XM_011515727.2 | 1742 | Intron | XP_011514029.1 | |||
XM_017011663.1 | 1742 | Silent Mutation | GGC,GGT | G,G 552 | XP_016867152.1 | |
XM_017011664.1 | 1742 | Silent Mutation | GGC,GGT | G,G 271 | XP_016867153.1 | |
XM_017011665.1 | 1742 | Silent Mutation | GGC,GGT | G,G 271 | XP_016867154.1 |