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ATGCTCACTGTGTCGGAGGAGCTGC[C/T]GTTTGACAACGTGGATGGTGGTGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 190030 MIM: 600988 | ||||||||||||||||||||||||||||||||||||||
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) - 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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FES - FES proto-oncogene, tyrosine kinase | ||||||
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There are no transcripts associated with this gene. |
MAN2A2 - mannosidase alpha class 2A member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320977.1 | 584 | Missense Mutation | CCG,CTG | P,L 139 | NP_001307906.1 | |
NM_006122.3 | 584 | Missense Mutation | CCG,CTG | P,L 139 | NP_006113.2 | |
XM_005254910.3 | 584 | Missense Mutation | CCG,CTG | P,L 139 | XP_005254967.1 | |
XM_011521565.2 | 584 | Intron | XP_011519867.1 | |||
XM_011521566.2 | 584 | Intron | XP_011519868.1 | |||
XM_017022184.1 | 584 | Missense Mutation | CCG,CTG | P,L 139 | XP_016877673.1 | |
XM_017022185.1 | 584 | Missense Mutation | CCG,CTG | P,L 139 | XP_016877674.1 |