Product Details

SNP ID
rs142927190
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:71719324 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGCTCCCGCGTGAGGCTGCTGCCC[A/C]TCCTGGGCGCCGCCCTGCTGCTGAT
Phenotype
MIM: 602606
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
CARTPT PubMed Links

Gene Details

Gene
CARTPT
Gene Name
CART prepropeptide
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004291.3 162 Missense Mutation ATC,CTC I11L NP_004282.1

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