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TCGTGGCTGTACTGCTGAAGCCACC[A/G]GTTCTTCAGAGTCTGGAGTGGAGAA
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 1509 | Missense Mutation | CGG,TGG | R,W 362 | NP_077008.2 | |
XM_011528274.1 | 1509 | Missense Mutation | CGG,TGG | R,W 409 | XP_011526576.1 | |
XM_011528275.1 | 1509 | Missense Mutation | CGG,TGG | R,W 362 | XP_011526577.1 | |
XM_011528276.1 | 1509 | Missense Mutation | CGG,TGG | R,W 353 | XP_011526578.1 | |
XM_011528277.1 | 1509 | Missense Mutation | CGG,TGG | R,W 409 | XP_011526579.1 | |
XM_011528278.1 | 1509 | Missense Mutation | CGG,TGG | R,W 409 | XP_011526580.1 | |
XM_011528279.1 | 1509 | Missense Mutation | CGG,TGG | R,W 317 | XP_011526581.1 | |
XM_011528280.1 | 1509 | Missense Mutation | CGG,TGG | R,W 409 | XP_011526582.1 | |
XM_011528281.1 | 1509 | Missense Mutation | CGG,TGG | R,W 409 | XP_011526583.1 | |
XM_011528282.1 | 1509 | Missense Mutation | CGG,TGG | R,W 409 | XP_011526584.1 | |
XM_011528283.1 | 1509 | Missense Mutation | CGG,TGG | R,W 409 | XP_011526585.1 | |
XM_011528284.1 | 1509 | Missense Mutation | CGG,TGG | R,W 409 | XP_011526586.1 | |
XM_011528285.1 | 1509 | Missense Mutation | CGG,TGG | R,W 353 | XP_011526587.1 | |
XM_017027285.1 | 1509 | Missense Mutation | CGG,TGG | R,W 409 | XP_016882774.1 | |
XM_017027286.1 | 1509 | Missense Mutation | CGG,TGG | R,W 306 | XP_016882775.1 | |
XM_017027287.1 | 1509 | Missense Mutation | CGG,TGG | R,W 270 | XP_016882776.1 | |
XM_017027288.1 | 1509 | Missense Mutation | CGG,TGG | R,W 362 | XP_016882777.1 | |
XM_017027289.1 | 1509 | Missense Mutation | CGG,TGG | R,W 317 | XP_016882778.1 | |
XM_017027290.1 | 1509 | Missense Mutation | CGG,TGG | R,W 306 | XP_016882779.1 | |
XM_017027291.1 | 1509 | Missense Mutation | CGG,TGG | R,W 270 | XP_016882780.1 | |
XM_017027292.1 | 1509 | Missense Mutation | CGG,TGG | R,W 306 | XP_016882781.1 |
SLC25A41 - solute carrier family 25 member 41 | ||||||
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There are no transcripts associated with this gene. |