Product Details

SNP ID: rs190020175
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:77040157 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCCTCAACCTCACGCTCAAGCACCT[A/G]CACTTGCTCGACTGGCTGGCTGCAC
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	744	Silent Mutation	CTA,CTG	L202L	NP_619651.3