Product Details

SNP ID
rs118113194
Assay Type
Functionally tested
NCBI dbSNP Submissions
28
Location
Chr.1:153299209 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCCATCCAACCCCTTCATACACGC[C/T]ACCATCCTGGCCCACCAGGAAGCTT
Phenotype
MIM: 608197
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PGLYRP3 PubMed Links

Gene Details

Gene
PGLYRP3
Gene Name
peptidoglycan recognition protein 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_052891.2 1233 Missense Mutation AGC,GGC S251G NP_443123.1
XM_011509118.1 1233 Missense Mutation AGC,GGC S287G XP_011507420.1
XM_011509119.1 1233 Missense Mutation AGC,GGC S251G XP_011507421.1
XM_011509120.2 1233 Missense Mutation AGC,GGC S249G XP_011507422.1

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