Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCACTAGAGGGCGCCAGCTCACCT[C/T]CCCTGTCAGAAGCAGATCCTCCCCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 611797 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
UQCC1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
UQCC1 - ubiquinol-cytochrome c reductase complex assembly factor 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184977.1 | 902 | Missense Mutation | NP_001171906.1 | |||
NM_018244.4 | 902 | Missense Mutation | NP_060714.3 | |||
NM_199487.2 | 902 | Missense Mutation | NP_955781.2 | |||
XM_011528877.1 | 902 | Missense Mutation | XP_011527179.1 | |||
XM_011528878.1 | 902 | Missense Mutation | XP_011527180.1 | |||
XM_011528879.1 | 902 | Missense Mutation | XP_011527181.1 | |||
XM_011528880.1 | 902 | Missense Mutation | XP_011527182.1 | |||
XM_011528881.2 | 902 | Missense Mutation | XP_011527183.1 | |||
XM_011528882.1 | 902 | Missense Mutation | XP_011527184.1 | |||
XM_011528883.1 | 902 | Missense Mutation | XP_011527185.1 | |||
XM_011528884.1 | 902 | Missense Mutation | XP_011527186.1 |