Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTTTTTCTCCTGTATGACTTCTCA[C/T]ATGAAGAGCAAGGGATGCAATTCGA
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 1174 | Missense Mutation | ATG,GTG | M,V 345 | NP_689697.2 | |
XM_006723046.2 | 1174 | Missense Mutation | ATG,GTG | M,V 369 | XP_006723109.1 | |
XM_006723047.3 | 1174 | Missense Mutation | ATG,GTG | M,V 369 | XP_006723110.1 | |
XM_006723048.3 | 1174 | Missense Mutation | ATG,GTG | M,V 369 | XP_006723111.1 | |
XM_011526538.2 | 1174 | Missense Mutation | ATG,GTG | M,V 369 | XP_011524840.1 | |
XM_011526539.2 | 1174 | Missense Mutation | ATG,GTG | M,V 345 | XP_011524841.1 | |
XM_017026376.1 | 1174 | Missense Mutation | ATG,GTG | M,V 345 | XP_016881865.1 | |
XM_017026377.1 | 1174 | Missense Mutation | ATG,GTG | M,V 345 | XP_016881866.1 | |
XM_017026378.1 | 1174 | Missense Mutation | ATG,GTG | M,V 309 | XP_016881867.1 | |
XM_017026379.1 | 1174 | Missense Mutation | ATG,GTG | M,V 186 | XP_016881868.1 | |
XM_017026380.1 | 1174 | Missense Mutation | ATG,GTG | M,V 186 | XP_016881869.1 | |
XM_017026381.1 | 1174 | Missense Mutation | ATG,GTG | M,V 186 | XP_016881870.1 | |
XM_017026382.1 | 1174 | Missense Mutation | ATG,GTG | M,V 186 | XP_016881871.1 |