Product Details

SNP ID: rs200446406
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:77040195 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGCTGGCTGCACGCTGCCCGCACG[C/G]GCGCTTTCTGCTCAGCGGCGACGAC
Phenotype: MIM: 615315
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: B3GNT6 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138706.4	782	Missense Mutation	GCG,GGG	A215G	NP_619651.3