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AAATTAAAGTATCTCACTCCAAGAG[A/C]GCAACCTTTAACTGTTATGCTCTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610586 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGAP24 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ARHGAP24 - Rho GTPase activating protein 24 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001025616.2 | Intron | NP_001020787.2 | ||||
NM_001042669.1 | Intron | NP_001036134.1 | ||||
NM_001287805.1 | Intron | NP_001274734.1 | ||||
NM_031305.2 | Intron | NP_112595.2 | ||||
XM_011532300.2 | Intron | XP_011530602.1 | ||||
XM_017008679.1 | Intron | XP_016864168.1 |