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TAGAATATTAAGGATGAATTCAGGA[A/G]GGCCTGAGACCATGGAAAACTTGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
7 submissions
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Phenotype: |
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Literature Links: |
ZCCHC17 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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ZCCHC17 - zinc finger CCHC-type containing 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282566.1 | 236 | Intron | NP_001269495.1 | |||
NM_001282567.1 | 236 | Intron | NP_001269496.1 | |||
NM_001282568.1 | 236 | Missense Mutation | AGG,GGG | R,G 5 | NP_001269497.1 | |
NM_001282569.1 | 236 | UTR 5 | NP_001269498.1 | |||
NM_001282570.1 | 236 | Intron | NP_001269499.1 | |||
NM_001282571.1 | 236 | UTR 5 | NP_001269500.1 | |||
NM_001282572.1 | 236 | Missense Mutation | AGG,GGG | R,G 5 | NP_001269501.1 | |
NM_001282573.1 | 236 | UTR 5 | NP_001269502.1 | |||
NM_001282574.1 | 236 | Missense Mutation | AGG,GGG | R,G 5 | NP_001269503.1 | |
NM_016505.3 | 236 | Missense Mutation | AGG,GGG | R,G 5 | NP_057589.2 | |
XM_006710681.3 | 236 | UTR 5 | XP_006710744.1 | |||
XM_011541567.2 | 236 | Missense Mutation | AGG,GGG | R,G 5 | XP_011539869.1 |