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CTTGGAGACATGTCCCAGGTCTGCC[A/G]GAGAGAACCCTGCCAGGCAGCTGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610591 MIM: 611466 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGAP27 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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ARHGAP27 - Rho GTPase activating protein 27 | ||||||
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There are no transcripts associated with this gene. |
PLEKHM1 - pleckstrin homology and RUN domain containing M1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014798.2 | Intron | NP_055613.1 | ||||
XM_006722201.3 | Intron | XP_006722264.1 | ||||
XM_011525523.2 | Intron | XP_011523825.1 | ||||
XM_011525524.1 | Intron | XP_011523826.1 | ||||
XM_011525525.1 | Intron | XP_011523827.1 | ||||
XM_011525526.1 | Intron | XP_011523828.1 | ||||
XM_011525528.2 | Intron | XP_011523830.1 | ||||
XM_017025451.1 | Intron | XP_016880940.1 | ||||
XM_017025452.1 | Intron | XP_016880941.1 | ||||
XM_017025453.1 | Intron | XP_016880942.1 | ||||
XM_017025454.1 | Intron | XP_016880943.1 |