Product Details

SNP ID
rs201852965
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:51994584 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATGCCCGGAAACTCATCCCCTAAG[A/G]GACTATTCCCTGGTGACCTGGGCCA
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LRRC66 PubMed Links

Gene Details

Gene
LRRC66
Gene Name
leucine rich repeat containing 66
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001024611.2 4172 Missense Mutation CCC,CTC P813L NP_001019782.1
XM_011534383.2 4172 Missense Mutation CCC,CTC P865L XP_011532685.1
XM_017008162.1 4172 Missense Mutation CCC,CTC P577L XP_016863651.1

View Full Product Details