Product Details

SNP ID
rs200207595
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:174493293 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAAATGGCATTCAGTCTCACACCAC[G/T]GTTCATAAGATTAGCAGCCAACTGC
Phenotype
MIM: 601688
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
HPGD PubMed Links

Gene Details

Gene
HPGD
Gene Name
hydroxyprostaglandin dehydrogenase 15-(NAD)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000860.5 697 Missense Mutation AGT,CGT S174R NP_000851.2
NM_001145816.2 697 Intron NP_001139288.1
NM_001256301.1 697 Missense Mutation AGT,CGT S53R NP_001243230.1
NM_001256305.1 697 Intron NP_001243234.1
NM_001256306.1 697 Missense Mutation AGT,CGT S106R NP_001243235.1
NM_001256307.1 697 Missense Mutation AGT,CGT S53R NP_001243236.1
XM_011531907.1 697 Intron XP_011530209.1

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