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ACCTCCAGAGCTTGACAGGGTGTTT[G/T]CGTAGGTGCTAACTAAATGTCTGAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
32 submissions
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Phenotype: |
MIM: 603270 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ATP5F1 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)
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SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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ATP5F1 - ATP synthase, H+ transporting, mitochondrial Fo complex subunit B1 | ||||||
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There are no transcripts associated with this gene. |
C1orf162 - chromosome 1 open reading frame 162 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300834.1 | Intron | NP_001287763.1 | ||||
NM_001300835.1 | Intron | NP_001287764.1 | ||||
NM_174896.3 | Intron | NP_777556.1 | ||||
XM_011540712.2 | Intron | XP_011539014.1 | ||||
XM_017000323.1 | Intron | XP_016855812.1 | ||||
XM_017000324.1 | Intron | XP_016855813.1 |
Set Membership: |
HapMap |