Product Details

SNP ID: rs146828783
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:78971986 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TAGGGGTAGTATCTGTAGTCAGAGG[G/T]GGCTTGGAAGTAATCAGAAGAATAT
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	1527	Missense Mutation	ACC,CCC	T450P	NP_005558.1