Product Details

SNP ID: rs16989521
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.21:32576841 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AGTAGGTGTTGCTCTTCTGTCTTGA[C/T]GTCTCCTGGAAAGATTTTTATCTCT
Phenotype: MIM: 608365
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: TCP10L PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_144659.5	697	Missense Mutation			NP_653260.1