Product Details

SNP ID
rs200129477
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:51994588 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCGGAAACTCATCCCCTAAGGGAC[A/T]ATTCCCTGGTGACCTGGGCCAGGGT
Phenotype
Polymorphism
A/T, Transversion 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 4168 Missense Mutation AGT,TGT S812C NP_001019782.1
XM_011534383.2 4168 Missense Mutation AGT,TGT S864C XP_011532685.1
XM_017008162.1 4168 Missense Mutation AGT,TGT S576C XP_016863651.1

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