Product Details

SNP ID
rs139033679
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:39383742 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATCTCCAATGATTCAGAACTCACG[G/T]CCGTCGCTGCTGCAACCCCAAGATG
Phenotype
MIM: 610819
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC25A38 PubMed Links

Gene Details

Gene
SLC25A38
Gene Name
solute carrier family 25 member 38
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017875.2 418 Silent Mutation CGG,CGT R6R NP_060345.2
XM_006713214.1 418 UTR 5 XP_006713277.1
XM_011533869.2 418 Intron XP_011532171.1
XM_017006710.1 418 Silent Mutation CGG,CGT R6R XP_016862199.1

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