Product Details

SNP ID: rs16890915
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:38677131 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ACTGCTTGAAAACCAGAATGACTGA[A/G]CAGTTAGGTGAAAAGGAACAGCTGA
Phenotype: MIM: 138750
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: GLO1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006708.2	841	UTR 3			NP_006699.2