Product Details

SNP ID: rs61734384
Assay Type: DME
NCBI dbSNP Submissions: NA
Location: Chr.6:52834166 on Build GRCh38
Set Membership: DME Validated Inventoried
Context Sequence [VIC/FAM]: TTTTTCAAAGGCAGGGAAGTAGCGA[C/T]TTTTTATTTTCTCTTTGACCAAGGC
Phenotype: MIM: 607605
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: GSTA5 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153699.1	459	Missense Mutation	AAT,AGT	N130S	NP_714543.1