Product Details

SNP ID: rs10230212
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:75932002 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ACCTGCTGCTAGGCCTCTGTGCACA[C/T]AGTGCTTTGTGGAATTGCTCCCGTC
Phenotype: MIM: 124015
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: POR PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000941.2		Intron			NP_000932.3