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GTGGCATTTTAAATTCTCTAATTTC[A/C]TATCCTTGGGACACATCAACTTAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611629 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NAV3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
NAV3 - neuron navigator 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001024383.1 | Intron | NP_001019554.1 | ||||
NM_014903.5 | Intron | NP_055718.4 | ||||
XM_005269215.3 | Intron | XP_005269272.1 | ||||
XM_011538940.2 | Intron | XP_011537242.1 | ||||
XM_011538941.2 | Intron | XP_011537243.1 | ||||
XM_011538944.2 | Intron | XP_011537246.1 | ||||
XM_017020164.1 | Intron | XP_016875653.1 | ||||
XM_017020165.1 | Intron | XP_016875654.1 | ||||
XM_017020166.1 | Intron | XP_016875655.1 | ||||
XM_017020167.1 | Intron | XP_016875656.1 | ||||
XM_017020168.1 | Intron | XP_016875657.1 | ||||
XM_017020169.1 | Intron | XP_016875658.1 | ||||
XM_017020170.1 | Intron | XP_016875659.1 | ||||
XM_017020171.1 | Intron | XP_016875660.1 | ||||
XM_017020172.1 | Intron | XP_016875661.1 | ||||
XM_017020173.1 | Intron | XP_016875662.1 | ||||
XM_017020174.1 | Intron | XP_016875663.1 | ||||
XM_017020175.1 | Intron | XP_016875664.1 |