Product Details

SNP ID
rs201717641
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:51994993 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTTGTTAGCAGGAGTGACATCCA[A/G]GCCACTGTCCCATCTTGGAGGAAAG
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 3763 Silent Mutation CTG,TTG L677L NP_001019782.1
XM_011534383.2 3763 Silent Mutation CTG,TTG L729L XP_011532685.1
XM_017008162.1 3763 Silent Mutation CTG,TTG L441L XP_016863651.1

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