Product Details

SNP ID
rs201543108
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:119410222 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCGTTCTCTGCTGGCTCCCTTCTT[A/G]TTTACATGAACCTGGAGAAAATCTG
Phenotype
MIM: 300641
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC25A43 PubMed Links

Gene Details

Gene
SLC25A43
Gene Name
solute carrier family 25 member 43
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_145305.2 659 Missense Mutation ATT,GTT I184V NP_660348.2
XM_017029340.1 659 Missense Mutation ATT,GTT I184V XP_016884829.1
XM_017029341.1 659 Missense Mutation ATT,GTT I184V XP_016884830.1

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