Product Details

SNP ID
rs200817852
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:40773980 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGATAGAGAATATTCCGAAGACTTC[C/T]CAATGTTCTGTTTTCTGGGTTTAGT
Phenotype
MIM: 606795
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC25A17 PubMed Links

Gene Details

Gene
SLC25A17
Gene Name
solute carrier family 25 member 17
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282726.1 937 Missense Mutation AGA,GGA R208G NP_001269655.1
NM_001282727.1 937 Missense Mutation AGA,GGA R172G NP_001269656.1
NM_006358.3 937 Missense Mutation AGA,GGA R245G NP_006349.1

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