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ATGCCAGGACTACATTGTCACGCTT[A/G]TTTTCACATAGTTCACTCAAGGAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 616725 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DDX60L PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
DDX60L - DEAD-box helicase 60-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012967.2 | 3572 | Silent Mutation | AAC,AAT | N,N 1673 | NP_001012985.2 | |
NM_001291510.1 | 3572 | Intron | NP_001278439.1 | |||
XM_005263341.4 | 3572 | Silent Mutation | AAC,AAT | N,N 1674 | XP_005263398.2 | |
XM_005263342.2 | 3572 | Silent Mutation | AAC,AAT | N,N 1674 | XP_005263399.2 | |
XM_005263343.2 | 3572 | Silent Mutation | AAC,AAT | N,N 1674 | XP_005263400.2 | |
XM_005263345.4 | 3572 | Silent Mutation | AAC,AAT | N,N 1674 | XP_005263402.2 | |
XM_006714408.2 | 3572 | Silent Mutation | AAC,AAT | N,N 1674 | XP_006714471.1 | |
XM_011532402.2 | 3572 | Silent Mutation | AAC,AAT | N,N 1674 | XP_011530704.1 | |
XM_011532403.2 | 3572 | Silent Mutation | AAC,AAT | N,N 1674 | XP_011530705.1 | |
XM_011532404.1 | 3572 | Silent Mutation | AAC,AAT | N,N 1642 | XP_011530706.1 | |
XM_011532405.1 | 3572 | Silent Mutation | AAC,AAT | N,N 1641 | XP_011530707.1 | |
XM_011532406.1 | 3572 | Silent Mutation | AAC,AAT | N,N 1639 | XP_011530708.1 | |
XM_011532409.2 | 3572 | Silent Mutation | AAC,AAT | N,N 1060 | XP_011530711.1 | |
XM_017008829.1 | 3572 | Silent Mutation | AAC,AAT | N,N 1642 | XP_016864318.1 | |
XM_017008830.1 | 3572 | Silent Mutation | AAC,AAT | N,N 1623 | XP_016864319.1 | |
XM_017008831.1 | 3572 | Silent Mutation | AAC,AAT | N,N 1060 | XP_016864320.1 |