Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTACAATACTTGCAATTTGCTCTG[A/G]AAAAACAATTCCCAAGGCATAGGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605196 | ||||||||||||||||||||
Literature Links: |
COQ3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
COQ3 - coenzyme Q3, methyltransferase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017421.3 | 826 | Missense Mutation | CCA,TCA | P,S 267 | NP_059117.3 | |
XM_005267018.4 | 826 | Missense Mutation | CCA,TCA | P,S 186 | XP_005267075.1 | |
XM_006715500.3 | 826 | Missense Mutation | CCA,TCA | P,S 308 | XP_006715563.1 | |
XM_011535898.2 | 826 | Missense Mutation | CCA,TCA | P,S 227 | XP_011534200.1 | |
XM_011535899.1 | 826 | Missense Mutation | CCA,TCA | P,S 148 | XP_011534201.1 | |
XM_017010933.1 | 826 | Missense Mutation | CCA,TCA | P,S 148 | XP_016866422.1 |