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Search Thermo Fisher Scientific
AGCCAGGAGGAAGAAAGAATGGCTG[T/G]TGGGCTTCTTAAAGCCATGTACCAG
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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There are no transcripts associated with this gene. |
ZNF570 - zinc finger protein 570 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300993.2 | 295 | Missense Mutation | GGT,GTT | G,V 59 | NP_001287922.1 | |
NM_001321991.1 | 295 | Missense Mutation | GGT,GTT | G,V 3 | NP_001308920.1 | |
NM_001321992.1 | 295 | Intron | NP_001308921.1 | |||
NM_001321993.1 | 295 | UTR 5 | NP_001308922.1 | |||
NM_001321994.1 | 295 | Intron | NP_001308923.1 | |||
NM_144694.3 | 295 | Missense Mutation | GGT,GTT | G,V 3 | NP_653295.1 | |
XM_011526544.2 | 295 | Missense Mutation | GGT,GTT | G,V 3 | XP_011524846.1 | |
XM_011526545.2 | 295 | Intron | XP_011524847.1 |