Product Details

SNP ID: rs182310862
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:77040508 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACATGGGCATGTGTCTGGAGCGCGC[C/T]GGCCTGGCGCCCAGCGGCCACGAGG
Phenotype: MIM: 615315
Polymorphism: C/T, Transition 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	1095	Silent Mutation	GCC,GCT	A319A	NP_619651.3