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ACAGGCATGTGGCACCACGCAGTCT[A/G]AAGTTGGTGAAGGAGACTGCACTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600326 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DDX6 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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DDX6 - DEAD-box helicase 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001257191.2 | 4238 | Intron | NP_001244120.1 | |||
NM_004397.5 | 4238 | Intron | NP_004388.2 | |||
XM_005271417.3 | 4238 | Intron | XP_005271474.1 | |||
XM_011542644.1 | 4238 | UTR 3 | XP_011540946.1 | |||
XM_011542645.1 | 4238 | UTR 3 | XP_011540947.1 | |||
XM_017017251.1 | 4238 | Intron | XP_016872740.1 |