Product Details

SNP ID
rs141472970
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:71440190 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGTTGCTGAGGGGCTGCCCCACAC[A/C]CTGTCATTGCGAGCCCGACGGCAGG
Phenotype
MIM: 606667
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
LGR5 PubMed Links

Gene Details

Gene
LGR5
Gene Name
leucine rich repeat containing G protein-coupled receptor 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001277226.1 421 Missense Mutation CAC,CCC H37P NP_001264155.1
NM_001277227.1 421 Missense Mutation CAC,CCC H37P NP_001264156.1
NM_003667.3 421 Missense Mutation CAC,CCC H37P NP_003658.1

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