Product Details

SNP ID: rs78919852
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:62206505 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGTGTCCTTGATACCTTTATCTCAT[C/T]TCTCTATTTTTTTTCCCTTCCCCAA
Phenotype: MIM: 605581
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: B3GNT2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001319075.1		Intron			NP_001306004.1
NM_006577.5		Intron			NP_006568.2

There are no transcripts associated with this gene.