Product Details

SNP ID
rs181132618
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:36104059 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTTTTCAGACTTTAAACATCATTA[A/C]ATATGTCACTGCGAGACATCGAGAG
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
LMBRD2 PubMed Links

Gene Details

Gene
LMBRD2
Gene Name
LMBR1 domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001007527.1 2932 Missense Mutation TGT,TTT C692F NP_001007528.1
XM_011514162.2 2932 Missense Mutation TGT,TTT C692F XP_011512464.1
XM_017010024.1 2932 Missense Mutation TGT,TTT C471F XP_016865513.1

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