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CTCCCACACCCACTGATGCCGAAGG[A/G]CTGCCCCAGCAGCAGCAGCTGCCGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300292 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FOXP3 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
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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FOXP3 - forkhead box P3 | ||||||
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There are no transcripts associated with this gene. |
PPP1R3F - protein phosphatase 1 regulatory subunit 3F | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184745.1 | 921 | Intron | NP_001171674.1 | |||
NM_033215.4 | 921 | Silent Mutation | GGA,GGG | G,G 298 | NP_149992.3 | |
XM_005272687.3 | 921 | Silent Mutation | GGA,GGG | G,G 298 | XP_005272744.1 | |
XM_017029932.1 | 921 | Intron | XP_016885421.1 | |||
XM_017029933.1 | 921 | Intron | XP_016885422.1 | |||
XM_017029934.1 | 921 | Silent Mutation | GGA,GGG | G,G 298 | XP_016885423.1 | |
XM_017029935.1 | 921 | Silent Mutation | GGA,GGG | G,G 298 | XP_016885424.1 |