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Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613369 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC47 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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CCDC47 - coiled-coil domain containing 47 | ||||||
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There are no transcripts associated with this gene. |
DDX42 - DEAD-box helicase 42 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_007372.3 | Intron | NP_031398.2 | ||||
NM_203499.2 | Intron | NP_987095.1 | ||||
XM_006721657.1 | Intron | XP_006721720.1 | ||||
XM_011524259.2 | Intron | XP_011522561.1 | ||||
XM_017024111.1 | Intron | XP_016879600.1 | ||||
XM_017024112.1 | Intron | XP_016879601.1 |