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GCTCCTCTTCCTTCCTTTATACCAG[T/C]CCTCGTCCCAGGTGAACTTGGTTTC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300859 MIM: 300292 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC22 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)
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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
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CCDC22 - coiled-coil domain containing 22 | ||||||
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There are no transcripts associated with this gene. |
FOXP3 - forkhead box P3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114377.1 | Intron | NP_001107849.1 | ||||
NM_014009.3 | Intron | NP_054728.2 | ||||
XM_006724533.2 | Intron | XP_006724596.2 | ||||
XM_011543916.2 | Intron | XP_011542218.1 | ||||
XM_017029565.1 | Intron | XP_016885054.1 | ||||
XM_017029566.1 | Intron | XP_016885055.1 | ||||
XM_017029567.1 | Intron | XP_016885056.1 |