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GGTTTCTCACCAGTATGAGTTTTCC[A/G]ATGTTGAATAAGGTTTGAGCCAGTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF573 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)
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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)
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EUR
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AMR
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ZNF573 - zinc finger protein 573 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001172689.1 | 1401 | Missense Mutation | CGG,TGG | R,W 401 | NP_001166160.1 | |
NM_001172690.1 | 1401 | Missense Mutation | CGG,TGG | R,W 489 | NP_001166161.1 | |
NM_001172691.1 | 1401 | Missense Mutation | CGG,TGG | R,W 487 | NP_001166162.1 | |
NM_001172692.1 | 1401 | Missense Mutation | CGG,TGG | R,W 401 | NP_001166163.1 | |
NM_152360.3 | 1401 | Missense Mutation | CGG,TGG | R,W 431 | NP_689573.3 | |
XM_011526446.2 | 1401 | Missense Mutation | CGG,TGG | R,W 504 | XP_011524748.1 | |
XM_017026275.1 | 1401 | Missense Mutation | CGG,TGG | R,W 504 | XP_016881764.1 | |
XM_017026276.1 | 1401 | Missense Mutation | CGG,TGG | R,W 504 | XP_016881765.1 | |
XM_017026277.1 | 1401 | Missense Mutation | CGG,TGG | R,W 502 | XP_016881766.1 | |
XM_017026278.1 | 1401 | Missense Mutation | CGG,TGG | R,W 433 | XP_016881767.1 | |
XM_017026279.1 | 1401 | Missense Mutation | CGG,TGG | R,W 433 | XP_016881768.1 | |
XM_017026280.1 | 1401 | Missense Mutation | CGG,TGG | R,W 401 | XP_016881769.1 | |
XM_017026281.1 | 1401 | Missense Mutation | CGG,TGG | R,W 401 | XP_016881770.1 |
Set Membership: |
HapMap |