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- SNP ID:
- rs148409263
- Gene
-
DDX55TMED2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.12: 123606150 - 123606150 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
TTCTGAGAAGAGAAGAGAAGTTAAA[A/G]AAGAGTCAGGTGAGGACAACAAAAG
Genomic Map
Back To TopAssay Details
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 | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| DDX55 - DEAD-box helicase 55 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_020936.2 | 250 | Silent Mutation | AAA,AAG | K,K 79 | NP_065987.1 | |
| XM_011538608.2 | 250 | Silent Mutation | AAA,AAG | K,K 79 | XP_011536910.1 | |
| XM_017019710.1 | 250 | Silent Mutation | AAA,AAG | K,K 79 | XP_016875199.1 | |
| XM_017019711.1 | 250 | Silent Mutation | AAA,AAG | K,K 41 | XP_016875200.1 | |
| XM_017019712.1 | 250 | Silent Mutation | AAA,AAG | K,K 36 | XP_016875201.1 | |
| XM_017019713.1 | 250 | Silent Mutation | AAA,AAG | K,K 36 | XP_016875202.1 | |
| XM_017019714.1 | 250 | Silent Mutation | AAA,AAG | K,K 36 | XP_016875203.1 | |
| XM_017019715.1 | 250 | Silent Mutation | AAA,AAG | K,K 79 | XP_016875204.1 | |
| XM_017019716.1 | 250 | Silent Mutation | AAA,AAG | K,K 79 | XP_016875205.1 | |
| XM_017019717.1 | 250 | UTR 5 | XP_016875206.1 | |||
| XM_017019718.1 | 250 | UTR 5 | XP_016875207.1 | |||
| XM_017019719.1 | 250 | UTR 5 | XP_016875208.1 | |||
| XM_017019720.1 | 250 | UTR 5 | XP_016875209.1 | |||
| XM_017019721.1 | 250 | Silent Mutation | AAA,AAG | K,K 79 | XP_016875210.1 | |
| TMED2 - transmembrane p24 trafficking protein 2 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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