Product Details

SNP ID
rs141707260
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:195571331 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCTCTGTGAGGTTAACTGGGGTGG[C/T]TTCACCTTCGATTTGATTCACAGTT
Phenotype
MIM: 107740
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
APOD PubMed Links

Gene Details

Gene
APOD
Gene Name
apolipoprotein D
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001647.3 642 Missense Mutation ACC,GCC T94A NP_001638.1

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