Product Details

SNP ID: rs1537234
Assay Type: Functionally tested
NCBI dbSNP Submissions: 58
Location: Chr.1:109737199 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AAGGAAAATACACCAAATCTTATAA[A/C]GACCCCAACCCAGTCCAACAGATGC
Phenotype: MIM: 138390
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: GSTM3 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000849.4		Intron			NP_000840.2