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GTGGAGCGCCCGGGGCTCTGGACCC[A/G]CGCTGCCAGATAACAATGCTCTCGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614902 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGAP33 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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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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ARHGAP33 - Rho GTPase activating protein 33 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001172630.1 | 1471 | Intron | NP_001166101.1 | |||
NM_052948.3 | 1471 | Intron | NP_443180.2 | |||
XM_005258488.1 | 1471 | Intron | XP_005258545.1 | |||
XM_006722999.1 | 1471 | Intron | XP_006723062.1 | |||
XM_006723003.2 | 1471 | Intron | XP_006723066.1 | |||
XM_011526416.1 | 1471 | Intron | XP_011524718.1 | |||
XM_011526417.1 | 1471 | Intron | XP_011524719.1 | |||
XM_011526418.1 | 1471 | Intron | XP_011524720.1 | |||
XM_011526419.1 | 1471 | Intron | XP_011524721.1 | |||
XM_011526420.1 | 1471 | Intron | XP_011524722.1 | |||
XM_011526421.2 | 1471 | Silent Mutation | CCA,CCG | P,P 14 | XP_011524723.1 | |
XM_017026238.1 | 1471 | Silent Mutation | CCA,CCG | P,P 14 | XP_016881727.1 |
PROSER3 - proline and serine rich 3 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |