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CCCAGAAGAGTCTTTTTGAATTATT[A/G]TTGATGAAAGTAATCGCTGTTCCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
8 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 | |||
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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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DDX59 - DEAD-box helicase 59 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031725.5 | 2066 | Silent Mutation | AAC,AAT | N,N 550 | NP_001026895.2 | |
NM_001320181.1 | 2066 | Intron | NP_001307110.1 | |||
NM_001320182.1 | 2066 | Silent Mutation | AAC,AAT | N,N 436 | NP_001307111.1 | |
XM_005245519.1 | 2066 | Silent Mutation | AAC,AAT | N,N 507 | XP_005245576.1 | |
XM_005245521.2 | 2066 | Silent Mutation | AAC,AAT | N,N 466 | XP_005245578.1 | |
XM_006711562.1 | 2066 | Intron | XP_006711625.1 | |||
XM_011510035.2 | 2066 | Silent Mutation | AAC,AAT | N,N 550 | XP_011508337.1 | |
XM_017002431.1 | 2066 | Intron | XP_016857920.1 | |||
XM_017002432.1 | 2066 | Silent Mutation | AAC,AAT | N,N 550 | XP_016857921.1 |