Product Details

SNP ID
rs202127516
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:74942714 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCCTCCAAGGGGTGGGTTACCTCC[A/G]GGGAACAGCATCGCCGCACCTGCCA
Phenotype
MIM: 601121
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PGF PubMed Links

Gene Details

Gene
PGF
Gene Name
placental growth factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001207012.1 1027 Missense Mutation CGG,TGG R148W NP_001193941.1
NM_001293643.1 1027 Missense Mutation CGG,TGG R168W NP_001280572.1
NM_002632.5 1027 Missense Mutation CGG,TGG R169W NP_002623.2

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