Product Details

SNP ID
rs188099064
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:49560017 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGCATCCCGGCTCAGTCGAATGTT[C/T]TGGGTCCCATAGCCCGAGGCCGCTG
Phenotype
MIM: 616759
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
NOSIP PubMed Links

Gene Details

Gene
NOSIP
Gene Name
nitric oxide synthase interacting protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001270960.1 228 Silent Mutation CAA,CAG Q31Q NP_001257889.1
NM_015953.4 228 Silent Mutation CAA,CAG Q31Q NP_057037.1
XM_005258964.4 228 Silent Mutation CAA,CAG Q31Q XP_005259021.1
XM_006723235.3 228 Silent Mutation CAA,CAG Q31Q XP_006723298.1
XM_011527015.2 228 Silent Mutation CAA,CAG Q32Q XP_011525317.1
XM_011527017.2 228 Silent Mutation CAA,CAG Q32Q XP_011525319.1
XM_017026851.1 228 Silent Mutation CAA,CAG Q31Q XP_016882340.1
XM_017026852.1 228 Silent Mutation CAA,CAG Q31Q XP_016882341.1

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