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CCTGGATCTCCTCAAAGTTCATCAG[A/G]TTGTTGGCCGTGTCAGACCAGGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616621 | ||||||||||||||||||||
Literature Links: |
DDX27 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 |
DDX27 - DEAD-box helicase 27 | ||||||
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There are no transcripts associated with this gene. |
ZNFX1 - zinc finger NFX1-type containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021035.2 | 4894 | Silent Mutation | AAC,AAT | N,N 1907 | NP_066363.1 | |
XM_006723836.1 | 4894 | Silent Mutation | AAC,AAT | N,N 1907 | XP_006723899.1 | |
XM_011528924.1 | 4894 | Silent Mutation | AAC,AAT | N,N 1857 | XP_011527226.1 | |
XM_017027971.1 | 4894 | Silent Mutation | AAC,AAT | N,N 1189 | XP_016883460.1 |