Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GATGCCGGGAAAACTCCGTAGTGAC[A/G]CTGGTTTGGAATCAGACACCGCAAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 606357 MIM: 610373 | ||||||||||||||||||||
Literature Links: |
DDX21 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 |
DDX21 - DEAD-box helicase 21 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256910.1 | 4344 | Intron | NP_001243839.1 | |||
NM_004728.3 | 4344 | Missense Mutation | ACT,GCT | T,A 9 | NP_004719.2 | |
XM_011540336.1 | 4344 | Missense Mutation | ACT,GCT | T,A 9 | XP_011538638.1 | |
XM_017016910.1 | 4344 | Intron | XP_016872399.1 |
DDX50 - DEAD-box helicase 50 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024045.1 | 4344 | Intron | NP_076950.1 | |||
XM_005270148.2 | 4344 | Intron | XP_005270205.1 | |||
XM_011540144.2 | 4344 | Intron | XP_011538446.1 | |||
XM_017016626.1 | 4344 | UTR 3 | XP_016872115.1 | |||
XM_017016627.1 | 4344 | Intron | XP_016872116.1 | |||
XM_017016628.1 | 4344 | Intron | XP_016872117.1 | |||
XM_017016629.1 | 4344 | Intron | XP_016872118.1 | |||
XM_017016630.1 | 4344 | Intron | XP_016872119.1 |