Product Details

SNP ID
rs890488
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:55751345 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGCAGTCGCGGAAGGGACAGGGGCG[C/G]GTCTTCTCCGGCTCAGGAAGGAGCT
Phenotype
MIM: 606055
Polymorphism
C/G, Transversion 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_001102402.2 216 UTR 5 NP_001095872.1
NM_021213.3 216 Intron NP_067036.2
XM_005257549.1 216 Intron XP_005257606.1
XM_005257550.3 216 Intron XP_005257607.1
XM_017024913.1 216 UTR 5 XP_016880402.1

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