Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTGTGCGCATCCCTGGAGGCCCAG[C/T]GGTGGCCAACAGTGTGGCACGGAAG
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 190030 MIM: 136950 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
FES 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese)
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EUR
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AMR
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FES - FES proto-oncogene, tyrosine kinase | ||||||
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There are no transcripts associated with this gene. |
FURIN - furin, paired basic amino acid cleaving enzyme | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289823.1 | 354 | Missense Mutation | GCG,GTG | A,V 43 | NP_001276752.1 | |
NM_001289824.1 | 354 | Missense Mutation | GCG,GTG | A,V 43 | NP_001276753.1 | |
NM_002569.3 | 354 | Missense Mutation | GCG,GTG | A,V 43 | NP_002560.1 |
Set Membership: |
HapMap |