Product Details

SNP ID
rs201684569
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:34052544 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCGCCGCGCCGGCTTCTCAGCAC[C/T]CCGCAACCGGCACCGGCGCTGTCCA
Phenotype
MIM: 601178
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CAPRIN1 PubMed Links

Gene Details

Gene
CAPRIN1
Gene Name
cell cycle associated protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005898.4 313 Missense Mutation CCC,TCC P42S NP_005889.3
NM_203364.2 313 Missense Mutation CCC,TCC P42S NP_976240.1
XM_017017749.1 313 Missense Mutation CCC,TCC P42S XP_016873238.1

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