Product Details

SNP ID: rs145820349
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:78971691 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGTGCTCTTCGAGCTGTTGGTGTCC[A/T]GGGCACTGGGAATCGCAGCCTTCCA
Phenotype: MIM: 600626
Polymorphism: A/T, Transversion substitution
Allele Nomenclature
Literature Links: LGALS3BP PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005567.3	1822	Missense Mutation	CAG,CTG	Q548L	NP_005558.1