Product Details

SNP ID: rs149820790
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:17802568 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TTTAGCCTGGAGGTCGAAGCCTCTC[A/G]GAGGTGACATTTCAGGGGAAGCCTA
Phenotype: MIM: 605863
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: B3GNT3 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014256.3		Intron			NP_055071.2
XM_011527626.2		Intron			XP_011525928.1