Product Details

SNP ID
rs146118434
Assay Type
Functionally tested
NCBI dbSNP Submissions
23
Location
Chr.1:153330916 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCACACTGGATCAGGTCTTGGGCTG[C/T]CTCTAGTGCTGCAGCATTGGGTGGT
Phenotype
MIM: 608198
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PGLYRP4 PubMed Links

Gene Details

Gene
PGLYRP4
Gene Name
peptidoglycan recognition protein 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020393.3 1333 Missense Mutation ACA,GCA T325A NP_065126.2
XM_011509789.2 1333 Missense Mutation ACA,GCA T325A XP_011508091.1
XM_011509790.1 1333 Missense Mutation ACA,GCA T325A XP_011508092.1
XM_011509791.2 1333 Missense Mutation ACA,GCA T321A XP_011508093.1
XM_011509792.1 1333 Intron XP_011508094.1
XM_011509793.2 1333 Missense Mutation ACA,GCA T157A XP_011508095.1

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