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AGAGTCTGTACAGGTGAAGCCTGAG[A/C]CTTTTTTCCTTTGGCCCTTGTTTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610373 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DDX50 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
|
DDX50 - DEAD-box helicase 50 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024045.1 | Intron | NP_076950.1 | ||||
XM_005270148.2 | Intron | XP_005270205.1 | ||||
XM_011540144.2 | Intron | XP_011538446.1 | ||||
XM_017016626.1 | Intron | XP_016872115.1 | ||||
XM_017016627.1 | Intron | XP_016872116.1 | ||||
XM_017016628.1 | Intron | XP_016872117.1 | ||||
XM_017016629.1 | Intron | XP_016872118.1 | ||||
XM_017016630.1 | Intron | XP_016872119.1 |