Product Details

SNP ID
rs144644967
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:154537417 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCAAAGACCCAGGTTGCACAGCTG[C/T]GTGAACTCTCTGAAAATTGTAGCCA
Phenotype
MIM: 605961
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PLRG1 PubMed Links

Gene Details

Gene
PLRG1
Gene Name
pleiotropic regulator 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001201564.1 1452 Missense Mutation ACA,GCA T443A NP_001188493.1
NM_002669.3 1452 Missense Mutation ACA,GCA T452A NP_002660.1

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