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AAGGCTTTTCCACATTTACTACAGT[C/T]GAAGGGTTTCTCACCTGTATGTCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613904 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF569 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
|
ZNF569 - zinc finger protein 569 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152484.2 | 2044 | Missense Mutation | AAC,GAC | N,D 635 | NP_689697.2 | |
XM_006723046.2 | 2044 | Missense Mutation | AAC,GAC | N,D 659 | XP_006723109.1 | |
XM_006723047.3 | 2044 | Missense Mutation | AAC,GAC | N,D 659 | XP_006723110.1 | |
XM_006723048.3 | 2044 | Missense Mutation | AAC,GAC | N,D 659 | XP_006723111.1 | |
XM_011526538.2 | 2044 | Missense Mutation | AAC,GAC | N,D 659 | XP_011524840.1 | |
XM_011526539.2 | 2044 | Missense Mutation | AAC,GAC | N,D 635 | XP_011524841.1 | |
XM_017026376.1 | 2044 | Missense Mutation | AAC,GAC | N,D 635 | XP_016881865.1 | |
XM_017026377.1 | 2044 | Missense Mutation | AAC,GAC | N,D 635 | XP_016881866.1 | |
XM_017026378.1 | 2044 | Missense Mutation | AAC,GAC | N,D 599 | XP_016881867.1 | |
XM_017026379.1 | 2044 | Missense Mutation | AAC,GAC | N,D 476 | XP_016881868.1 | |
XM_017026380.1 | 2044 | Missense Mutation | AAC,GAC | N,D 476 | XP_016881869.1 | |
XM_017026381.1 | 2044 | Missense Mutation | AAC,GAC | N,D 476 | XP_016881870.1 | |
XM_017026382.1 | 2044 | Missense Mutation | AAC,GAC | N,D 476 | XP_016881871.1 |