Product Details

SNP ID: rs487098
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.6:122444760 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: TAAAATAGTCAAACAAATTTGTTTT[C/T]ACTCTTCATTTCACAACTATAGAGC
Phenotype: MIM: 614548
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: SERINC1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020755.3	1790	UTR 3			NP_065806.1