Product Details

SNP ID: rs184467713
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:747548 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCTGGACCAGCTCAAGCAGTTCACC[A/G]CCGTGGTGGCCGACACGGGCGACTT
Phenotype: MIM: 602063
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: TALDO1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006755.1	117	Missense Mutation	ACC,GCC	T23A	NP_006746.1