Product Details

SNP ID: rs61729727
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:78971723 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGGAATCGCAGCCTTCCAGCCCTC[A/G]AAATCGGTGACGTCTGCCACGAAGA
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	1790	Silent Mutation	TTC,TTT	F537F	NP_005558.1