Search Thermo Fisher Scientific
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GCGGCATGGAGCGGGAGCCGGGCGC[C/G]GCGGGAGTTCGCCGGGCTCTGGGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612819 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DDX51 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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DDX51 - DEAD-box helicase 51 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_175066.3 | 88 | Intron | NP_778236.2 | |||
XM_011538256.1 | 88 | Intron | XP_011536558.1 |
NOC4L - nucleolar complex associated 4 homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024078.2 | 88 | Silent Mutation | GCC,GCG | A,A 7 | NP_076983.1 | |
XM_017019960.1 | 88 | Silent Mutation | GCC,GCG | A,A 7 | XP_016875449.1 |