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TTCCGAGGGTTCTGCTACCAGGAGG[C/T]GGCAGGTCCCCGAGAAGCCCTGGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF324 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 |
ZNF324 - zinc finger protein 324 | ||||||
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There are no transcripts associated with this gene. |
ZNF446 - zinc finger protein 446 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304453.1 | 491 | Missense Mutation | GCG,GTG | A,V 37 | NP_001291382.1 | |
NM_017908.3 | 491 | Missense Mutation | GCG,GTG | A,V 37 | NP_060378.1 | |
XM_005259052.4 | 491 | Missense Mutation | GCG,GTG | A,V 37 | XP_005259109.1 | |
XM_005259053.4 | 491 | Missense Mutation | GCG,GTG | A,V 37 | XP_005259110.1 | |
XM_006723266.3 | 491 | Missense Mutation | GCG,GTG | A,V 37 | XP_006723329.1 | |
XM_017026949.1 | 491 | Missense Mutation | GCG,GTG | A,V 37 | XP_016882438.1 | |
XM_017026950.1 | 491 | Missense Mutation | GCG,GTG | A,V 37 | XP_016882439.1 |