Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGCTGAGCCTGCTCATCCGGGAAC[A/G]GCAGCAGCTTCGCAAGACCTACAGC
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
FES - FES proto-oncogene, tyrosine kinase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143783.1 | 406 | Intron | NP_001137255.1 | |||
NM_001143784.1 | 406 | Missense Mutation | CAG,CGG | Q,R 109 | NP_001137256.1 | |
NM_001143785.1 | 406 | Intron | NP_001137257.1 | |||
NM_002005.3 | 406 | Missense Mutation | CAG,CGG | Q,R 109 | NP_001996.1 | |
XM_005254880.1 | 406 | Intron | XP_005254937.1 | |||
XM_005254882.1 | 406 | Missense Mutation | CAG,CGG | Q,R 109 | XP_005254939.1 | |
XM_017022005.1 | 406 | Missense Mutation | CAG,CGG | Q,R 109 | XP_016877494.1 | |
XM_017022006.1 | 406 | Intron | XP_016877495.1 | |||
XM_017022007.1 | 406 | Missense Mutation | CAG,CGG | Q,R 109 | XP_016877496.1 | |
XM_017022008.1 | 406 | Intron | XP_016877497.1 | |||
XM_017022009.1 | 406 | Missense Mutation | CAG,CGG | Q,R 109 | XP_016877498.1 | |
XM_017022010.1 | 406 | Intron | XP_016877499.1 |
FURIN - furin, paired basic amino acid cleaving enzyme | ||||||
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There are no transcripts associated with this gene. |