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- SNP ID:
- rs145212772
- Gene
-
ARHGAP12 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.10: 31807003 - 31807003 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
CCTAAAATGCCCTGAACTGACTTCC[A/G]CTAACTAAAACTCCAGTATATCACA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610577
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Literature Links: |
ARHGAP12 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
|
| ARHGAP12 - Rho GTPase activating protein 12 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001270695.1 | 3278 | UTR 3 | NP_001257624.1 | |||
| NM_001270696.1 | 3278 | UTR 3 | NP_001257625.1 | |||
| NM_001270697.1 | 3278 | UTR 3 | NP_001257626.1 | |||
| NM_001270698.1 | 3278 | UTR 3 | NP_001257627.1 | |||
| NM_001270699.1 | 3278 | UTR 3 | NP_001257628.1 | |||
| NM_018287.6 | 3278 | UTR 3 | NP_060757.4 | |||
| XM_005252644.1 | 3278 | UTR 3 | XP_005252701.1 | |||
| XM_011519761.1 | 3278 | UTR 3 | XP_011518063.1 | |||
| XM_017016954.1 | 3278 | UTR 3 | XP_016872443.1 | |||
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