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CGGCCCGCTGCCCGCTGAGCCCCTC[A/C]TGGCCTTGGCCGGGCCGGCAGCCGC
Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
12 submissions
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Phenotype: |
MIM: 601094 | ||||||||||||||||||||||||||
Literature Links: |
FOXE3 PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese)
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EUR - Not Available | |||||
AMR - Not Available |
FOXE3 - forkhead box E3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012186.2 | 1103 | Missense Mutation | ATG,CTG | M,L 287 | NP_036318.1 |
LINC01389 - long intergenic non-protein coding RNA 1389 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |