Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C5orf58 PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
C5orf58 - chromosome 5 open reading frame 58 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001102609.2 | 189 | Missense Mutation | CCT,CGT | P,R 26 | NP_001096079.1 | |
NM_001305393.1 | 189 | Missense Mutation | CCT,CGT | P,R 26 | NP_001292322.1 | |
NM_001305394.1 | 189 | Missense Mutation | CCT,CGT | P,R 26 | NP_001292323.1 | |
NM_001305395.1 | 189 | Missense Mutation | CCT,CGT | P,R 26 | NP_001292324.1 | |
NM_001305396.1 | 189 | Missense Mutation | CCT,CGT | P,R 26 | NP_001292325.1 | |
NM_001305397.1 | 189 | Missense Mutation | CCT,CGT | P,R 26 | NP_001292326.1 | |
XM_011534432.2 | 189 | Missense Mutation | CCT,CGT | P,R 65 | XP_011532734.1 | |
XM_017009029.1 | 189 | Missense Mutation | CCT,CGT | P,R 65 | XP_016864518.1 | |
XM_017009030.1 | 189 | Missense Mutation | CCT,CGT | P,R 65 | XP_016864519.1 | |
XM_017009031.1 | 189 | Missense Mutation | CCT,CGT | P,R 26 | XP_016864520.1 | |
XM_017009032.1 | 189 | Missense Mutation | CCT,CGT | P,R 26 | XP_016864521.1 | |
XM_017009033.1 | 189 | Missense Mutation | CCT,CGT | P,R 26 | XP_016864522.1 |