Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACCATCAGACAAAAGAGCCCCATGG[C/T]CTCCGAGAGGGCAAAGCCCAGAATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603193 | ||||||||||||||||||||
Literature Links: |
ATP5G2 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 |
ATP5G2 - ATP synthase, H+ transporting, mitochondrial Fo complex subunit C2 (subunit 9) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002031.2 | 688 | Missense Mutation | ACC,GCC | T,A 141 | NP_001002031.1 | |
NM_005176.5 | 688 | Missense Mutation | NP_005167.2 | |||
XM_017019460.1 | 688 | Missense Mutation | ACC,GCC | T,A 182 | XP_016874949.1 | |
XM_017019461.1 | 688 | Missense Mutation | ACC,GCC | T,A 141 | XP_016874950.1 | |
XM_017019462.1 | 688 | Missense Mutation | ACC,GCC | T,A 125 | XP_016874951.1 |