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CTCAAGGAGCCGCCCCCGGCGGCGT[C/T]CAAGGGCGCCCCGGCCACCCCCCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602402 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FOXC2 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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FOXC2 - forkhead box C2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005251.2 | 657 | Missense Mutation | TCC,TTC | S,F 191 | NP_005242.1 |
FOXC2-AS1 - FOXC2 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |