Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF517 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) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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ZNF517 - zinc finger protein 517 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317936.1 | 663 | Missense Mutation | CCG,CTG | P,L 6 | NP_001304865.1 | |
NM_213605.2 | 663 | Missense Mutation | CCG,CTG | P,L 6 | NP_998770.2 | |
XM_011517014.2 | 663 | Missense Mutation | CCG,CTG | P,L 6 | XP_011515316.1 | |
XM_011517015.2 | 663 | Missense Mutation | CCG,CTG | P,L 6 | XP_011515317.1 | |
XM_011517017.2 | 663 | Silent Mutation | CCC,CCT | P,P 26 | XP_011515319.1 | |
XM_017013384.1 | 663 | Intron | XP_016868873.1 |
Set Membership: |
HapMap |