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ACAAGACTCCTCAGAACACTGAGTT[A/C]TGTCAGATTCCCCATTCAAGTCTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609096 MIM: 610894 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FBXO22 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
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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FBXO22 - F-box protein 22 | ||||||
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There are no transcripts associated with this gene. |
NRG4 - neuregulin 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_138573.3 | Intron | NP_612640.1 | ||||
XM_017021937.1 | Intron | XP_016877426.1 | ||||
XM_017021938.1 | Intron | XP_016877427.1 | ||||
XM_017021939.1 | Intron | XP_016877428.1 | ||||
XM_017021940.1 | Intron | XP_016877429.1 | ||||
XM_017021941.1 | Intron | XP_016877430.1 | ||||
XM_017021942.1 | Intron | XP_016877431.1 | ||||
XM_017021943.1 | Intron | XP_016877432.1 | ||||
XM_017021944.1 | Intron | XP_016877433.1 | ||||
XM_017021945.1 | Intron | XP_016877434.1 | ||||
XM_017021946.1 | Intron | XP_016877435.1 | ||||
XM_017021947.1 | Intron | XP_016877436.1 | ||||
XM_017021948.1 | Intron | XP_016877437.1 |