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CGCTGGCCGAAGCGGACAAGGTCCG[A/G]CTGTCCTACCTGCACATCATGAGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608554 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NPAS4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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NPAS4 - neuronal PAS domain protein 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318804.1 | 284 | UTR 5 | NP_001305733.1 | |||
NM_178864.3 | 284 | Silent Mutation | CGA,CGG | R,R 36 | NP_849195.2 | |
XM_017017537.1 | 284 | Silent Mutation | CGA,CGG | R,R 113 | XP_016873026.1 | |
XM_017017538.1 | 284 | Intron | XP_016873027.1 | |||
XM_017017539.1 | 284 | Silent Mutation | CGA,CGG | R,R 36 | XP_016873028.1 |