Product Details

SNP ID: rs138232181
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:747536 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GATGGAGTCCGCGCTGGACCAGCTC[A/C]AGCAGTTCACCACCGTGGTGGCCGA
Phenotype: MIM: 602063
Polymorphism: A/C, Transversion 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	105	Missense Mutation	AAG,CAG	K19Q	NP_006746.1