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- SNP ID:
- rs146840425
- Gene
-
DHX34 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 47353279 - 47353279 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CCTCCAGGAAGGAGGAGAAAGACCC[C/T]GGACAGCCCAAGCACAGCATCCCAG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615475
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Literature Links: |
DHX34 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
|
| DHX34 - DEAH-box helicase 34 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_014681.5 | 547 | Silent Mutation | CCC,CCT | P,P 83 | NP_055496.2 | |
| XM_005259443.3 | 547 | Silent Mutation | CCC,CCT | P,P 83 | XP_005259500.1 | |
| XM_011527550.2 | 547 | Silent Mutation | CCC,CCT | P,P 83 | XP_011525852.1 | |
| XM_011527551.2 | 547 | Silent Mutation | CCC,CCT | P,P 83 | XP_011525853.1 | |
| XM_017027524.1 | 547 | UTR 5 | XP_016883013.1 | |||
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