Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCGTGAGCGAAGATGGCAAATCGG[A/G]CGACGAGCTGCTCTCCAGCAAGGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
14 submissions
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Phenotype: |
MIM: 611628 | ||||||||||||||||||||
Literature Links: |
NAV1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
NAV1 - neuron navigator 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167738.1 | 625 | Intron | NP_001161210.1 | |||
NM_020443.4 | 625 | Missense Mutation | GAC,GGC | D,G 200 | NP_065176.3 | |
XM_006711609.2 | 625 | Intron | XP_006711672.2 | |||
XM_006711610.2 | 625 | Intron | XP_006711673.2 | |||
XM_006711611.1 | 625 | Intron | XP_006711674.1 | |||
XM_011510097.1 | 625 | Missense Mutation | GAC,GGC | D,G 200 | XP_011508399.1 | |
XM_011510098.1 | 625 | Missense Mutation | GAC,GGC | D,G 200 | XP_011508400.1 | |
XM_011510099.1 | 625 | Missense Mutation | GAC,GGC | D,G 200 | XP_011508401.1 | |
XM_011510100.1 | 625 | Missense Mutation | GAC,GGC | D,G 200 | XP_011508402.1 | |
XM_011510101.1 | 625 | Missense Mutation | GAC,GGC | D,G 200 | XP_011508403.1 | |
XM_011510102.1 | 625 | Missense Mutation | GAC,GGC | D,G 200 | XP_011508404.1 | |
XM_017002751.1 | 625 | Missense Mutation | GAC,GGC | D,G 200 | XP_016858240.1 | |
XM_017002752.1 | 625 | Intron | XP_016858241.1 | |||
XM_017002753.1 | 625 | Missense Mutation | GAC,GGC | D,G 200 | XP_016858242.1 | |
XM_017002754.1 | 625 | Missense Mutation | GAC,GGC | D,G 200 | XP_016858243.1 |