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GGAACTCGAAGCGCAGGCTCTGCTC[A/G]GTGGTGTGGTGGCCCCGGGGCAGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600483 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FGF8 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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FGF8 - fibroblast growth factor 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206389.1 | 744 | Silent Mutation | ACC,ACT | T,T 110 | NP_001193318.1 | |
NM_006119.4 | 744 | Silent Mutation | ACC,ACT | T,T 185 | NP_006110.1 | |
NM_033163.3 | 744 | Silent Mutation | ACC,ACT | T,T 214 | NP_149353.1 | |
NM_033164.3 | 744 | Silent Mutation | ACC,ACT | T,T 203 | NP_149354.1 | |
NM_033165.3 | 744 | Silent Mutation | ACC,ACT | T,T 174 | NP_149355.1 |