Product Details

SNP ID
rs201625289
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:6444205 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCAGCGGGTAACTGGCTATCTGGC[C/T]GCAGGTGCTGGATATGGTACCGCAG
Phenotype
MIM: 608746 MIM: 610822
Polymorphism
C/T, Transition 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 1593 Missense Mutation AGC,GGC S390G NP_077008.2
XM_011528274.1 1593 Missense Mutation AGC,GGC S437G XP_011526576.1
XM_011528275.1 1593 Missense Mutation AGC,GGC S390G XP_011526577.1
XM_011528276.1 1593 Missense Mutation AGC,GGC S381G XP_011526578.1
XM_011528277.1 1593 Missense Mutation AGC,GGC S437G XP_011526579.1
XM_011528278.1 1593 Missense Mutation AGC,GGC S437G XP_011526580.1
XM_011528279.1 1593 Missense Mutation AGC,GGC S345G XP_011526581.1
XM_011528280.1 1593 Missense Mutation AGC,GGC S437G XP_011526582.1
XM_011528281.1 1593 Missense Mutation AGC,GGC S437G XP_011526583.1
XM_011528282.1 1593 Missense Mutation AGC,GGC S437G XP_011526584.1
XM_011528283.1 1593 Missense Mutation AGC,GGC S437G XP_011526585.1
XM_011528284.1 1593 Missense Mutation AGC,GGC S437G XP_011526586.1
XM_011528285.1 1593 Missense Mutation AGC,GGC S381G XP_011526587.1
XM_017027285.1 1593 Missense Mutation AGC,GGC S437G XP_016882774.1
XM_017027286.1 1593 Missense Mutation AGC,GGC S334G XP_016882775.1
XM_017027287.1 1593 Missense Mutation AGC,GGC S298G XP_016882776.1
XM_017027288.1 1593 Missense Mutation AGC,GGC S390G XP_016882777.1
XM_017027289.1 1593 Missense Mutation AGC,GGC S345G XP_016882778.1
XM_017027290.1 1593 Missense Mutation AGC,GGC S334G XP_016882779.1
XM_017027291.1 1593 Missense Mutation AGC,GGC S298G XP_016882780.1
XM_017027292.1 1593 Missense Mutation AGC,GGC S334G 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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