Product Details

SNP ID
rs199749627
Assay Type
Functionally tested
NCBI dbSNP Submissions
1
Location
Chr.1:201648927 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGGCCGCCCGCCTCCAACCTGCGC[A/C]AGCAGAAGTCACTCACCAACCTCTC
Phenotype
MIM: 611628
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
NAV1 PubMed Links

Gene Details

Gene
NAV1
Gene Name
neuron navigator 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001167738.1 285 Intron NP_001161210.1
NM_020443.4 285 Missense Mutation AAG,CAG K87Q NP_065176.3
XM_006711609.2 285 Intron XP_006711672.2
XM_006711610.2 285 Intron XP_006711673.2
XM_006711611.1 285 Intron XP_006711674.1
XM_011510097.1 285 Missense Mutation AAG,CAG K87Q XP_011508399.1
XM_011510098.1 285 Missense Mutation AAG,CAG K87Q XP_011508400.1
XM_011510099.1 285 Missense Mutation AAG,CAG K87Q XP_011508401.1
XM_011510100.1 285 Missense Mutation AAG,CAG K87Q XP_011508402.1
XM_011510101.1 285 Missense Mutation AAG,CAG K87Q XP_011508403.1
XM_011510102.1 285 Missense Mutation AAG,CAG K87Q XP_011508404.1
XM_017002751.1 285 Missense Mutation AAG,CAG K87Q XP_016858240.1
XM_017002752.1 285 Intron XP_016858241.1
XM_017002753.1 285 Missense Mutation AAG,CAG K87Q XP_016858242.1
XM_017002754.1 285 Missense Mutation AAG,CAG K87Q XP_016858243.1

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