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GACTTCTTCACACTCAGCGCTTTGA[C/T]ATGGATCTTCTCCAGGACAAATGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF563 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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ZNF563 - zinc finger protein 563 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_145276.2 | 546 | Missense Mutation | TAT,TGT | Y,C 103 | NP_660319.1 | |
XM_005259750.4 | 546 | Intron | XP_005259807.1 | |||
XM_005259751.3 | 546 | Intron | XP_005259808.1 | |||
XM_006722650.3 | 546 | Intron | XP_006722713.1 | |||
XM_006722651.3 | 546 | Intron | XP_006722714.1 | |||
XM_011527698.1 | 546 | Intron | XP_011526000.1 | |||
XM_011527699.2 | 546 | Missense Mutation | TAT,TGT | Y,C 66 | XP_011526001.1 | |
XM_011527700.2 | 546 | Intron | XP_011526002.1 | |||
XM_017026332.1 | 546 | Intron | XP_016881821.1 |