Product Details

SNP ID

rs144710000

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:153330874 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCACCAGCAGGTAGTTGGGAGTCA[A/G]GTACCCTTTGACCATGGCACACTGG

Phenotype

MIM: 608198

Polymorphism

A/G, 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	1375	Silent Mutation	CTG,TTG	L339L	NP_065126.2
XM_011509789.2	1375	Silent Mutation	CTG,TTG	L339L	XP_011508091.1
XM_011509790.1	1375	Silent Mutation	CTG,TTG	L339L	XP_011508092.1
XM_011509791.2	1375	Silent Mutation	CTG,TTG	L335L	XP_011508093.1
XM_011509792.1	1375	Intron			XP_011508094.1
XM_011509793.2	1375	Silent Mutation	CTG,TTG	L171L	XP_011508095.1

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