Product Details

SNP ID
rs200737083
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:6444226 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCCGCAGGTGCTGGATATGGTAC[C/T]GCAGGCCAGGAGCACGAGGATGCCT
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 1572 Missense Mutation NP_077008.2
XM_011528274.1 1572 Missense Mutation XP_011526576.1
XM_011528275.1 1572 Missense Mutation XP_011526577.1
XM_011528276.1 1572 Missense Mutation XP_011526578.1
XM_011528277.1 1572 Missense Mutation XP_011526579.1
XM_011528278.1 1572 Missense Mutation XP_011526580.1
XM_011528279.1 1572 Missense Mutation XP_011526581.1
XM_011528280.1 1572 Missense Mutation XP_011526582.1
XM_011528281.1 1572 Missense Mutation XP_011526583.1
XM_011528282.1 1572 Missense Mutation XP_011526584.1
XM_011528283.1 1572 Missense Mutation XP_011526585.1
XM_011528284.1 1572 Missense Mutation XP_011526586.1
XM_011528285.1 1572 Missense Mutation XP_011526587.1
XM_017027285.1 1572 Missense Mutation XP_016882774.1
XM_017027286.1 1572 Missense Mutation XP_016882775.1
XM_017027287.1 1572 Missense Mutation XP_016882776.1
XM_017027288.1 1572 Missense Mutation XP_016882777.1
XM_017027289.1 1572 Missense Mutation XP_016882778.1
XM_017027290.1 1572 Missense Mutation XP_016882779.1
XM_017027291.1 1572 Missense Mutation XP_016882780.1
XM_017027292.1 1572 Missense Mutation 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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