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GTAGGAAGGATGAAGGGGAGGCCTG[C/G]CTGAGCTGTCATCCCCCAGGTAATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608016 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
COA4 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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COA4 - cytochrome c oxidase assembly factor 4 homolog | ||||||
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There are no transcripts associated with this gene. |
PAAF1 - proteasomal ATPase associated factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001267803.1 | 91 | UTR 5 | NP_001254732.1 | |||
NM_001267804.1 | 91 | UTR 5 | NP_001254733.1 | |||
NM_001267805.1 | 91 | UTR 5 | NP_001254734.1 | |||
NM_001267806.1 | 91 | UTR 5 | NP_001254735.1 | |||
NM_025155.2 | 91 | Missense Mutation | TGC,TGG | C,W 23 | NP_079431.1 | |
XM_005274308.2 | 91 | Intron | XP_005274365.2 | |||
XM_005274309.1 | 91 | UTR 5 | XP_005274366.1 | |||
XM_017018357.1 | 91 | UTR 5 | XP_016873846.1 | |||
XM_017018358.1 | 91 | UTR 5 | XP_016873847.1 | |||
XM_017018359.1 | 91 | Intron | XP_016873848.1 |