Product Details

SNP ID
rs138598051
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:6444185 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCATGCGGGTCCGGACCAGGGCCAG[C/G]GGGTAACTGGCTATCTGGCCGCAGG
Phenotype
MIM: 608746 MIM: 610822
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
SLC25A23 PubMed Links

Gene Details

Gene
SLC25A23
Gene Name
solute carrier family 25 member 23
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_024103.2 1613 Silent Mutation CCC,CCG P396P NP_077008.2
XM_011528274.1 1613 Silent Mutation CCC,CCG P443P XP_011526576.1
XM_011528275.1 1613 Silent Mutation CCC,CCG P396P XP_011526577.1
XM_011528276.1 1613 Silent Mutation CCC,CCG P387P XP_011526578.1
XM_011528277.1 1613 Silent Mutation CCC,CCG P443P XP_011526579.1
XM_011528278.1 1613 Silent Mutation CCC,CCG P443P XP_011526580.1
XM_011528279.1 1613 Silent Mutation CCC,CCG P351P XP_011526581.1
XM_011528280.1 1613 Silent Mutation CCC,CCG P443P XP_011526582.1
XM_011528281.1 1613 Silent Mutation CCC,CCG P443P XP_011526583.1
XM_011528282.1 1613 Silent Mutation CCC,CCG P443P XP_011526584.1
XM_011528283.1 1613 Silent Mutation CCC,CCG P443P XP_011526585.1
XM_011528284.1 1613 Silent Mutation CCC,CCG P443P XP_011526586.1
XM_011528285.1 1613 Silent Mutation CCC,CCG P387P XP_011526587.1
XM_017027285.1 1613 Silent Mutation CCC,CCG P443P XP_016882774.1
XM_017027286.1 1613 Silent Mutation CCC,CCG P340P XP_016882775.1
XM_017027287.1 1613 Silent Mutation CCC,CCG P304P XP_016882776.1
XM_017027288.1 1613 Silent Mutation CCC,CCG P396P XP_016882777.1
XM_017027289.1 1613 Silent Mutation CCC,CCG P351P XP_016882778.1
XM_017027290.1 1613 Silent Mutation CCC,CCG P340P XP_016882779.1
XM_017027291.1 1613 Silent Mutation CCC,CCG P304P XP_016882780.1
XM_017027292.1 1613 Silent Mutation CCC,CCG P340P XP_016882781.1
Gene
SLC25A41
Gene Name
solute carrier family 25 member 41
There are no transcripts associated with this gene.

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