Product Details

SNP ID: rs201472381
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:100707179 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGATGAGCTGGAGCCAGAGACCGAC[A/C]CACGGGAGCCACTGACTCGGATCCG
Phenotype: MIM: 606113
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: POP7 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005837.2	611	Missense Mutation	ACA,CCA	T117P	NP_005828.2