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TTGGAGCGGGCACCCCGGCCGAAGG[A/C]GCCCTGCTGCAGCTCCTGGACGCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611665 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CFAP73 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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CFAP73 - cilia and flagella associated protein 73 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144872.1 | 1168 | UTR 3 | NP_001138344.1 | |||
XM_011538327.2 | 1168 | Intron | XP_011536629.1 |
DDX54 - DEAD-box helicase 54 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001111322.1 | 1168 | Missense Mutation | NP_001104792.1 | |||
NM_024072.3 | 1168 | Missense Mutation | NP_076977.3 |
MIR7106 - microRNA 7106 | ||||||
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There are no transcripts associated with this gene. |