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GCGATTCTTCGACCTCTGCAGCCCC[C/T]CTCAGGGGGCTCGGGGGACCCCTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608666 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PEX26 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) - Not Available | |||
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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PEX26 - peroxisomal biogenesis factor 26 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127649.2 | 242 | Silent Mutation | CCC,CCT | P,P 11 | NP_001121121.1 | |
NM_001199319.1 | 242 | Silent Mutation | CCC,CCT | P,P 11 | NP_001186248.1 | |
NM_017929.5 | 242 | Silent Mutation | CCC,CCT | P,P 11 | NP_060399.1 |