Product Details

SNP ID: rs201605703
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:77039907 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGCGCCGGCGGCCGAGGCGTGTTCC[C/T]GCTCCTGGCGGTGAAGTCGGCGCCT
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	494	Missense Mutation	CCG,CTG	P119L	NP_619651.3