Product Details

SNP ID: rs185015376
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:52840811 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGTAGTGGAGCTTGGGCTTCTCTGC[C/T]ATGATAGCAGTCTCCTGGAGGTTTC
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	73	Missense Mutation	ATA,ATG	I1M	NP_714543.1