Product Details

SNP ID

rs200031382

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15475628 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGCACTGAAGCTGGAGGTGTACTG[G/T]CTCCAGCCTCTGTAGAAGGACAAGG

Phenotype

MIM: 608199

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

PGLYRP2 PubMed Links

Gene Details

Gene

PGLYRP2

Gene Name

peptidoglycan recognition protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_052890.3	1175	Missense Mutation	ACA,CCA	T348P	NP_443122.3
XM_006722633.3	1175	Missense Mutation	ACA,CCA	T348P	XP_006722696.1

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