Product Details

SNP ID: rs2180314
Assay Type: DME
NCBI dbSNP Submissions: NA
Location: Chr.6:52752933 on Build GRCh38
Set Membership: HapMap DME Validated Inventoried
Context Sequence [VIC/FAM]: CTTGGCATCTTGTTCCTCAGGTTGA[C/G]TAAAGGGCAGAAGAAGGATCATTTC
Phenotype: MIM: 138360
Polymorphism: C/G, 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	485	Missense Mutation	ACT,AGT	T112S	NP_000837.3
XM_011514532.2	485	Intron			XP_011512834.1

There are no transcripts associated with this gene.