Product Details

SNP ID: rs148696353
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:78971688 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGAGGTGCTCTTCGAGCTGTTGGTG[G/T]CCAGGGCACTGGGAATCGCAGCCTT
Phenotype: MIM: 600626
Polymorphism: G/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	1825	Missense Mutation	GAC,GCC	D549A	NP_005558.1