Product Details

SNP ID: rs141503569
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:100707097 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCATCAACATCGCGCTGCAGCTGCA[A/G]GCGGGCAGCTTCGGGTCCTTGCAGG
Phenotype: MIM: 606113
Polymorphism: A/G, Transition 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	529	Silent Mutation	CAA,CAG	Q89Q	NP_005828.2