Product Details

SNP ID: rs457661
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:38165885 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GAGCCGCTGCCGCCGTCATGTCCGA[A/G]GACTCGAGCGCCCTGCCCTGGTCCA
Phenotype: MIM: 604046
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: OXSR1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005109.2	355	Silent Mutation	GAA,GAG	E3E	NP_005100.1
XM_005265638.2	355	UTR 5			XP_005265695.1
XM_011534331.2	355	Intron			XP_011532633.1
XM_017007601.1	355	Intron			XP_016863090.1
XM_017007602.1	355	UTR 5			XP_016863091.1