Product Details

SNP ID
rs200114975
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:20143562 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGTTGCTACTGTGGGCTGGGGGGC[C/T]GTGGCCAGCCCAAGGATGAGGTGGA
Phenotype
MIM: 616793
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PLA2G2F PubMed Links

Gene Details

Gene
PLA2G2F
Gene Name
phospholipase A2 group IIF
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_022819.3 377 Missense Mutation CGT,TGT R96C NP_073730.3
XM_011541955.1 377 Missense Mutation CGT,TGT R96C XP_011540257.1
XM_011541956.1 377 Missense Mutation CGT,TGT R96C XP_011540258.1

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