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- SNP ID:
- rs11588189
- Gene
-
ARHGAP30USF1 - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.1: 161049831 - 161049831 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
ATGACTGATCCTTTCAGACCAATGT[C/T]CCTAGTTATTGGCTTGCTACCTTAA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
33 submissions
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Phenotype: |
MIM: 614264
MIM: 191523
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Literature Links: |
ARHGAP30 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
|
| ARHGAP30 - Rho GTPase activating protein 30 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001025598.1 | Intron | NP_001020769.1 | ||||
| NM_001287600.1 | Intron | NP_001274529.1 | ||||
| NM_001287602.1 | Intron | NP_001274531.1 | ||||
| NM_181720.2 | Intron | NP_859071.2 | ||||
| XM_005245070.2 | Intron | XP_005245127.1 | ||||
| XM_005245073.3 | Intron | XP_005245130.1 | ||||
| XM_011509391.2 | Intron | XP_011507693.1 | ||||
| XM_017000960.1 | Intron | XP_016856449.1 | ||||
| USF1 - upstream transcription factor 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
Back To TopMore Information
Set Membership: |
HapMap
|
Panther Classification:
Gene Ontology Categories:
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