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Search Thermo Fisher Scientific
AGAATTACTTTTATCATGTTTTCTG[A/T]TAATATCCATAAGATTAGCTCCTGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
|
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Phenotype: |
MIM: 615464 | ||||||||||||||||||||
Literature Links: |
DDX59 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 |
DDX59 - DEAD-box helicase 59 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031725.5 | 2242 | Missense Mutation | AAC,ATC | N,I 609 | NP_001026895.2 | |
NM_001320181.1 | 2242 | Intron | NP_001307110.1 | |||
NM_001320182.1 | 2242 | Missense Mutation | AAC,ATC | N,I 495 | NP_001307111.1 | |
XM_005245519.1 | 2242 | Missense Mutation | AAC,ATC | N,I 566 | XP_005245576.1 | |
XM_005245521.2 | 2242 | Missense Mutation | AAC,ATC | N,I 525 | XP_005245578.1 | |
XM_006711562.1 | 2242 | Intron | XP_006711625.1 | |||
XM_011510035.2 | 2242 | Missense Mutation | AAC,ATC | N,I 609 | XP_011508337.1 | |
XM_017002431.1 | 2242 | Intron | XP_016857920.1 | |||
XM_017002432.1 | 2242 | Missense Mutation | AAC,ATC | N,I 609 | XP_016857921.1 |