Product Details

SNP ID: rs143986382
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:78971676 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCAGGGGAAGGAGGAGGTGCTCTTC[A/G]AGCTGTTGGTGTCCAGGGCACTGGG
Phenotype: MIM: 600626
Polymorphism: A/G, Transition 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	1837	Missense Mutation			NP_005558.1