Product Details

SNP ID: rs149640294
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:755962 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGCACAGATGCCCGCTTACCAGGAG[C/G]TGGTGGAGGAGGCGATTGCCTATGG
Phenotype: MIM: 602063
Polymorphism: C/G, 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	231	Missense Mutation	CTG,GTG	L61V	NP_006746.1