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GGGTCTTCATCAAGACCATCAGGCG[C/T]GATATCTTGTGAGTACCTGGCCCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612898 MIM: 604194 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
COQ4 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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COQ4 - coenzyme Q4 | ||||||
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There are no transcripts associated with this gene. |
SLC27A4 - solute carrier family 27 member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005094.3 | 311 | Silent Mutation | CGC,CGT | R,R 51 | NP_005085.2 | |
XM_017014222.1 | 311 | Silent Mutation | CGC,CGT | R,R 51 | XP_016869711.1 |