Product Details

SNP ID
rs148359917
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:150996516 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGAGCAGCTGCTGAGTCAGGCCC[A/G]GGACTTCATCAACCAGTACTACAGC
Phenotype
MIM: 163729
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
NOS3 PubMed Links

Gene Details

Gene
NOS3
Gene Name
nitric oxide synthase 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000603.4 436 Missense Mutation CAG,CGG Q128R NP_000594.2
NM_001160109.1 436 Missense Mutation CAG,CGG Q128R NP_001153581.1
NM_001160110.1 436 Missense Mutation CAG,CGG Q128R NP_001153582.1
NM_001160111.1 436 Missense Mutation CAG,CGG Q128R NP_001153583.1
XM_006716002.3 436 Missense Mutation CAG,CGG Q128R XP_006716065.1
XM_017012232.1 436 Missense Mutation CAG,CGG Q128R XP_016867721.1
XM_017012233.1 436 UTR 5 XP_016867722.1
XM_017012234.1 436 Missense Mutation CAG,CGG Q128R XP_016867723.1

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