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- SNP ID:
- rs11574637
- Gene
-
ITGAX - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.16: 31357553 - 31357553 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CGATCGCCCGCACGCTGCCGGACCT[C/T]TCCTGTGACCTTAACCTCTCCAAGC
Genomic Map
Back To TopAssay Details
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 151510
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Literature Links: |
ITGAX 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 | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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| ITGAX - integrin subunit alpha X | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_000887.4 | Intron | NP_000878.2 | ||||
| NM_001286375.1 | Intron | NP_001273304.1 | ||||
| XM_011545852.1 | Intron | XP_011544154.1 | ||||
| XM_011545854.1 | Intron | XP_011544156.1 | ||||
Back To TopMore Information
Set Membership: |
HapMap
|
Panther Classification:
Gene Ontology Categories:
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