Product Details

SNP ID: rs1894008
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:77037138 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GGGAAGCTAAGGAAAAGAGCATGAG[A/G]AGCGGCATAAATCTACGTAATTCAA
Phenotype: MIM: 615315
Polymorphism: A/G, 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		Intron			NP_619651.3