Product Details
- SNP ID
-
rs147732917
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
3
- Location
-
Chr.1:201648860 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGGCCAAGGCCAGCGCGGCTGAGCT[G/T]AAGGTCTTCAAGTCCGGCAGCGTGG
- Phenotype
-
MIM: 611628
- Polymorphism
- G/T, 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 |
218 |
Intron |
|
|
NP_001161210.1 |
NM_020443.4 |
218 |
Silent Mutation |
CTG,CTT |
L64L |
NP_065176.3 |
XM_006711609.2 |
218 |
Intron |
|
|
XP_006711672.2 |
XM_006711610.2 |
218 |
Intron |
|
|
XP_006711673.2 |
XM_006711611.1 |
218 |
Intron |
|
|
XP_006711674.1 |
XM_011510097.1 |
218 |
Silent Mutation |
CTG,CTT |
L64L |
XP_011508399.1 |
XM_011510098.1 |
218 |
Silent Mutation |
CTG,CTT |
L64L |
XP_011508400.1 |
XM_011510099.1 |
218 |
Silent Mutation |
CTG,CTT |
L64L |
XP_011508401.1 |
XM_011510100.1 |
218 |
Silent Mutation |
CTG,CTT |
L64L |
XP_011508402.1 |
XM_011510101.1 |
218 |
Silent Mutation |
CTG,CTT |
L64L |
XP_011508403.1 |
XM_011510102.1 |
218 |
Silent Mutation |
CTG,CTT |
L64L |
XP_011508404.1 |
XM_017002751.1 |
218 |
Silent Mutation |
CTG,CTT |
L64L |
XP_016858240.1 |
XM_017002752.1 |
218 |
Intron |
|
|
XP_016858241.1 |
XM_017002753.1 |
218 |
Silent Mutation |
CTG,CTT |
L64L |
XP_016858242.1 |
XM_017002754.1 |
218 |
Silent Mutation |
CTG,CTT |
L64L |
XP_016858243.1 |
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