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GTAGAATTAATTTCTCCCACCGAAA[T/C]ACTTTAAATCCTAGTAGGCTTTGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605812 | ||||||||||||||||||||
Literature Links: |
DDX19B 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 |
DDX19B - DEAD-box helicase 19B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001014449.2 | Intron | NP_001014449.1 | ||||
NM_001014451.2 | Intron | NP_001014451.1 | ||||
NM_001257172.1 | Intron | NP_001244101.1 | ||||
NM_001257173.1 | Intron | NP_001244102.1 | ||||
NM_001257174.1 | Intron | NP_001244103.1 | ||||
NM_001257175.1 | Intron | NP_001244104.1 | ||||
NM_007242.5 | Intron | NP_009173.1 | ||||
XM_006721127.2 | Intron | XP_006721190.1 | ||||
XM_011522832.2 | Intron | XP_011521134.1 | ||||
XM_011522833.2 | Intron | XP_011521135.1 | ||||
XM_011522834.2 | Intron | XP_011521136.1 | ||||
XM_017022890.1 | Intron | XP_016878379.1 |