Product Details

SNP ID
rs146793058
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:76659617 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCCCGGCTTCTTTAGGCTTTATAC[G/T]GTTGGTTAAACTTCTGCCGGCGGAC
Phenotype
MIM: 137207
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
LRRC32 PubMed Links

Gene Details

Gene
LRRC32
Gene Name
leucine rich repeat containing 32
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001128922.1 2308 Missense Mutation CAG,CCG Q659P NP_001122394.1
NM_005512.2 2308 Missense Mutation CAG,CCG Q659P NP_005503.1
XM_005273902.3 2308 Missense Mutation CAG,CCG Q659P XP_005273959.1
XM_005273903.4 2308 Missense Mutation CAG,CCG Q637P XP_005273960.2
XM_011544935.2 2308 Missense Mutation CAG,CCG Q659P XP_011543237.1
XM_017017527.1 2308 Missense Mutation CAG,CCG Q659P XP_016873016.1

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