Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGTGTGTTGAGGCAGTGTACTTTTT[G/T]GCGCTCAGTTACATATGCGTAGTAC
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 |
---|---|---|
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 |
DDX6 - DEAD-box helicase 6 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001257191.2 | 1244 | Intron | NP_001244120.1 | |||
NM_004397.5 | 1244 | Intron | NP_004388.2 | |||
XM_005271417.3 | 1244 | Missense Mutation | AAA,CAA | K,Q 320 | XP_005271474.1 | |
XM_011542644.1 | 1244 | Intron | XP_011540946.1 | |||
XM_011542645.1 | 1244 | Missense Mutation | AAA,CAA | K,Q 271 | XP_011540947.1 | |
XM_017017251.1 | 1244 | Intron | XP_016872740.1 |