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ACCTGCGTGCCGGCTGCCACCCACC[C/T]AGCCACTCCTCCTCAGGACAATGAA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616467 MIM: 608071 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
DPCD 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)
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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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DPCD - deleted in primary ciliary dyskinesia homolog (mouse) | ||||||
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There are no transcripts associated with this gene. |
FBXW4 - F-box and WD repeat domain containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323541.1 | Intron | NP_001310470.1 | ||||
NM_022039.3 | Intron | NP_071322.1 | ||||
XM_005270053.2 | Intron | XP_005270110.2 | ||||
XM_017016570.1 | Intron | XP_016872059.1 |