Product Details

SNP ID
rs190878117
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:102973585 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTCGTGTTGTCTGTTGGCACACTC[C/T]CAAGAGTTTGAACGGATACAAGAAT
Phenotype
MIM: 609080 MIM: 612133
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FBXL13 PubMed Links

Gene Details

Gene
FBXL13
Gene Name
F-box and leucine rich repeat protein 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001111038.1 Intron NP_001104508.1
NM_001287150.1 Intron NP_001274079.1
NM_145032.3 Intron NP_659469.3
XM_005250205.3 Intron XP_005250262.1
XM_005250207.3 Intron XP_005250264.1
XM_005250208.3 Intron XP_005250265.1
XM_005250209.2 Intron XP_005250266.1
XM_006715898.2 Intron XP_006715961.1
XM_011515928.2 Intron XP_011514230.1
XM_011515929.2 Intron XP_011514231.1
XM_011515930.2 Intron XP_011514232.1
XM_011515932.2 Intron XP_011514234.1
XM_017011850.1 Intron XP_016867339.1
XM_017011851.1 Intron XP_016867340.1
XM_017011852.1 Intron XP_016867341.1
XM_017011853.1 Intron XP_016867342.1
Gene
NFE4
Gene Name
nuclear factor, erythroid 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001085386.1 Intron NP_001078855.1

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