Product Details

SNP ID
rs201233687
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:99242434 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTGACGAAGTCATTGTCTATGTCC[A/G]ATGGGGTGGCAATCGCTTCAATTCC
Phenotype
MIM: 616547
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
LYG2 PubMed Links

Gene Details

Gene
LYG2
Gene Name
lysozyme g2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_175735.3 682 Missense Mutation TCG,TTG S190L NP_783862.2
XM_017003751.1 682 Missense Mutation TCG,TTG S190L XP_016859240.1

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