Product Details

SNP ID
rs35116632
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:55751110 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGCCCGGACTGCGGAAGGATGGAG[C/T]TGGCCGCCGGAAGCTTCTCGGAGGA
Phenotype
MIM: 606055
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PCTP PubMed Links

Gene Details

Gene
PCTP
Gene Name
phosphatidylcholine transfer protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001102402.2 132 UTR 5 NP_001095872.1
NM_021213.3 132 Silent Mutation CTG,TTG L3L NP_067036.2
XM_005257549.1 132 Silent Mutation CTG,TTG L3L XP_005257606.1
XM_005257550.3 132 Silent Mutation CTG,TTG L3L XP_005257607.1
XM_017024913.1 132 Intron XP_016880402.1

View Full Product Details