Product Details

SNP ID
rs141856398
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.8:103400460 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGTAAAAAATGTGAGACGTTTTCA[C/T]ATACCACAAAGGTAATACAGCAGGC
Phenotype
MIM: 610815
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SLC25A32 PubMed Links

Gene Details

Gene
SLC25A32
Gene Name
solute carrier family 25 member 32
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_030780.4 1297 Missense Mutation TAT,TGT Y300C NP_110407.2
XM_017013877.1 1297 Missense Mutation TAT,TGT Y168C XP_016869366.1

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