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CTCCCTGGGCTCAGATGGGGACTGC[A/G]CGGCCAACAGCCCGGCCGCGGGCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612788 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FOXQ1 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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FOXQ1 - forkhead box Q1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033260.3 | 404 | Missense Mutation | ACG,GCG | T,A 47 | NP_150285.3 |
LINC01394 - long intergenic non-protein coding RNA 1394 | ||||||
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There are no transcripts associated with this gene. |
LOC107986554 - uncharacterized LOC107986554 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_017011607.1 | 404 | Intron | XP_016867096.1 | |||
XM_017011608.1 | 404 | Intron | XP_016867097.1 | |||
XM_017011609.1 | 404 | Intron | XP_016867098.1 | |||
XM_017011610.1 | 404 | Intron | XP_016867099.1 | |||
XM_017011611.1 | 404 | Intron | XP_016867100.1 |