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GGTCACAGGTAGTGGCAAAACACTC[A/G]CTTTTGTCATCCCCATCCTGGAAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
DDX55 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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DDX55 - DEAD-box helicase 55 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020936.2 | 197 | Missense Mutation | ACT,GCT | T,A 62 | NP_065987.1 | |
XM_011538608.2 | 197 | Missense Mutation | ACT,GCT | T,A 62 | XP_011536910.1 | |
XM_017019710.1 | 197 | Missense Mutation | ACT,GCT | T,A 62 | XP_016875199.1 | |
XM_017019711.1 | 197 | Missense Mutation | ACT,GCT | T,A 24 | XP_016875200.1 | |
XM_017019712.1 | 197 | Missense Mutation | ACT,GCT | T,A 19 | XP_016875201.1 | |
XM_017019713.1 | 197 | Missense Mutation | ACT,GCT | T,A 19 | XP_016875202.1 | |
XM_017019714.1 | 197 | Missense Mutation | ACT,GCT | T,A 19 | XP_016875203.1 | |
XM_017019715.1 | 197 | Missense Mutation | ACT,GCT | T,A 62 | XP_016875204.1 | |
XM_017019716.1 | 197 | Missense Mutation | ACT,GCT | T,A 62 | XP_016875205.1 | |
XM_017019717.1 | 197 | UTR 5 | XP_016875206.1 | |||
XM_017019718.1 | 197 | UTR 5 | XP_016875207.1 | |||
XM_017019719.1 | 197 | UTR 5 | XP_016875208.1 | |||
XM_017019720.1 | 197 | UTR 5 | XP_016875209.1 | |||
XM_017019721.1 | 197 | Missense Mutation | ACT,GCT | T,A 62 | XP_016875210.1 |
TMED2 - transmembrane p24 trafficking protein 2 | ||||||
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There are no transcripts associated with this gene. |