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CTTTTCACAGATTTTTTACTTTTAG[A/G]AGTAGCTTTCTGTTTAGGTTTTTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 125264 | ||||||||||||||||||||
Literature Links: |
DEK 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 |
DEK - DEK proto-oncogene | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001134709.1 | 902 | Missense Mutation | CCT,TCT | P,S 237 | NP_001128181.1 | |
NM_003472.3 | 902 | Missense Mutation | CCT,TCT | P,S 271 | NP_003463.1 | |
XM_017011273.1 | 902 | Missense Mutation | CCT,TCT | P,S 271 | XP_016866762.1 |