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GCATGCGGGTCCGGACCAGGGCCAG[C/G]GGGTAACTGGCTATCTGGCCGCAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608746 MIM: 610822 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC25A23 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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SLC25A23 - solute carrier family 25 member 23 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024103.2 | 1613 | Silent Mutation | CCC,CCG | P,P 396 | NP_077008.2 | |
XM_011528274.1 | 1613 | Silent Mutation | CCC,CCG | P,P 443 | XP_011526576.1 | |
XM_011528275.1 | 1613 | Silent Mutation | CCC,CCG | P,P 396 | XP_011526577.1 | |
XM_011528276.1 | 1613 | Silent Mutation | CCC,CCG | P,P 387 | XP_011526578.1 | |
XM_011528277.1 | 1613 | Silent Mutation | CCC,CCG | P,P 443 | XP_011526579.1 | |
XM_011528278.1 | 1613 | Silent Mutation | CCC,CCG | P,P 443 | XP_011526580.1 | |
XM_011528279.1 | 1613 | Silent Mutation | CCC,CCG | P,P 351 | XP_011526581.1 | |
XM_011528280.1 | 1613 | Silent Mutation | CCC,CCG | P,P 443 | XP_011526582.1 | |
XM_011528281.1 | 1613 | Silent Mutation | CCC,CCG | P,P 443 | XP_011526583.1 | |
XM_011528282.1 | 1613 | Silent Mutation | CCC,CCG | P,P 443 | XP_011526584.1 | |
XM_011528283.1 | 1613 | Silent Mutation | CCC,CCG | P,P 443 | XP_011526585.1 | |
XM_011528284.1 | 1613 | Silent Mutation | CCC,CCG | P,P 443 | XP_011526586.1 | |
XM_011528285.1 | 1613 | Silent Mutation | CCC,CCG | P,P 387 | XP_011526587.1 | |
XM_017027285.1 | 1613 | Silent Mutation | CCC,CCG | P,P 443 | XP_016882774.1 | |
XM_017027286.1 | 1613 | Silent Mutation | CCC,CCG | P,P 340 | XP_016882775.1 | |
XM_017027287.1 | 1613 | Silent Mutation | CCC,CCG | P,P 304 | XP_016882776.1 | |
XM_017027288.1 | 1613 | Silent Mutation | CCC,CCG | P,P 396 | XP_016882777.1 | |
XM_017027289.1 | 1613 | Silent Mutation | CCC,CCG | P,P 351 | XP_016882778.1 | |
XM_017027290.1 | 1613 | Silent Mutation | CCC,CCG | P,P 340 | XP_016882779.1 | |
XM_017027291.1 | 1613 | Silent Mutation | CCC,CCG | P,P 304 | XP_016882780.1 | |
XM_017027292.1 | 1613 | Silent Mutation | CCC,CCG | P,P 340 | XP_016882781.1 |
SLC25A41 - solute carrier family 25 member 41 | ||||||
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There are no transcripts associated with this gene. |