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- SNP ID:
- rs10740055
- Gene
-
ARID5B - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.10: 61958720 - 61958720 on Build GRCh38
- Polymorphism:
- A/C, Transversion substitution
- Context Sequence [VIC/FAM]:
CTAGGAACTTATACTTAGTTCAAAC[A/C]CAGCTTTCCAAATAGAAACCCTGTG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608538
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Literature Links: |
ARID5B PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | ||||||
|---|---|---|---|---|---|---|---|---|
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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| ARID5B - AT-rich interaction domain 5B | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001244638.1 | Intron | NP_001231567.1 | ||||
| NM_032199.2 | Intron | NP_115575.1 | ||||
| XM_011540262.1 | Intron | XP_011538564.1 | ||||
| XM_017016765.1 | Intron | XP_016872254.1 | ||||
Back To TopMore Information
Set Membership: |
HapMap
|
Panther Classification:
Gene Ontology Categories:
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