Product Details

SNP ID: rs60332313
Assay Type: DME
NCBI dbSNP Submissions: NA
Location: Chr.6:52752894 on Build GRCh38
Set Membership: DME Validated Inventoried
Context Sequence [VIC/FAM]: GAAGTAGCGATTTTTTGTTTTCTCT[G/T]GGATCAAGGCAAGCTTGGCATCTTG
Phenotype: MIM: 138360
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: GSTA2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000846.4	524	Missense Mutation	CAA,CCA	Q125P	NP_000837.3
XM_011514532.2	524	Intron			XP_011512834.1

There are no transcripts associated with this gene.