Product Details

SNP ID
rs151020278
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:76659654 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCTGCCGGCGGACGCAGCAGCAGG[C/T]GGCCAGCGTGGTGAGGAGGATGGCA
Phenotype
MIM: 137207
Polymorphism
C/T, Transition 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 2271 Missense Mutation ACC,GCC T647A NP_001122394.1
NM_005512.2 2271 Missense Mutation ACC,GCC T647A NP_005503.1
XM_005273902.3 2271 Missense Mutation ACC,GCC T647A XP_005273959.1
XM_005273903.4 2271 Missense Mutation ACC,GCC T625A XP_005273960.2
XM_011544935.2 2271 Missense Mutation ACC,GCC T647A XP_011543237.1
XM_017017527.1 2271 Missense Mutation ACC,GCC T647A XP_016873016.1

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