Product Details

SNP ID: rs10075302
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:141303391 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AAGGGGCCATCCTTTTTAAGGATAC[A/C]CTTCACGACAGACCAAATTGTATTA
Phenotype: MIM: 608157
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: SLC25A2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031947.3	673	Missense Mutation			NP_114153.1