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Search Thermo Fisher Scientific
TCAAGGACTGTCCTTGGTATGACCG[C/T]GGCTTCTGCAAGCACGGTAGGTGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603052 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ATP5J2 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)
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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) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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ATP5J2 - ATP synthase, H+ transporting, mitochondrial Fo complex subunit F2 | ||||||
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There are no transcripts associated with this gene. |
ATP5J2-PTCD1 - ATP5J2-PTCD1 readthrough | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198879.1 | 505 | Intron | NP_001185808.1 |
CPSF4 - cleavage and polyadenylation specific factor 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001081559.2 | 505 | Silent Mutation | CGC,CGT | R,R 129 | NP_001075028.1 | |
NM_001318160.1 | 505 | Silent Mutation | CGC,CGT | R,R 129 | NP_001305089.1 | |
NM_001318161.1 | 505 | Silent Mutation | CGC,CGT | R,R 129 | NP_001305090.1 | |
NM_001318162.1 | 505 | Silent Mutation | CGC,CGT | R,R 76 | NP_001305091.1 | |
NM_006693.3 | 505 | Silent Mutation | CGC,CGT | R,R 129 | NP_006684.1 | |
XM_011515755.2 | 505 | Silent Mutation | CGC,CGT | R,R 129 | XP_011514057.1 | |
XM_011515756.2 | 505 | Silent Mutation | CGC,CGT | R,R 129 | XP_011514058.1 | |
XM_011515757.2 | 505 | Silent Mutation | CGC,CGT | R,R 129 | XP_011514059.1 | |
XM_017011700.1 | 505 | Silent Mutation | CGC,CGT | R,R 129 | XP_016867189.1 | |
XM_017011701.1 | 505 | Silent Mutation | CGC,CGT | R,R 129 | XP_016867190.1 | |
XM_017011702.1 | 505 | Silent Mutation | CGC,CGT | R,R 76 | XP_016867191.1 | |
XM_017011703.1 | 505 | Silent Mutation | CGC,CGT | R,R 76 | XP_016867192.1 |
Set Membership: |
HapMap |