Product Details

SNP ID: rs145528403
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:52831939 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCCAGGCTGCAGAAACTTCTTCACC[A/G]TGGGCAGGTTGCTGATTCTGGTTTT
Phenotype: MIM: 607605
Polymorphism: A/G, 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	648	Missense Mutation	ACG,ATG	T193M	NP_714543.1