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GGAGCCTGCTAAAGGGGTGCCCCGC[C/G]ACGCCCCTACCCCATCCGCCCCACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610591 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGAP27 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
|
ARHGAP27 - Rho GTPase activating protein 27 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282290.1 | Intron | NP_001269219.1 | ||||
NM_174919.3 | Intron | NP_777579.2 | ||||
NM_199282.2 | Intron | NP_954976.1 | ||||
XM_005257128.3 | Intron | XP_005257185.1 | ||||
XM_006721745.2 | Intron | XP_006721808.1 | ||||
XM_006721747.2 | Intron | XP_006721810.1 | ||||
XM_006721750.3 | Intron | XP_006721813.1 | ||||
XM_011524468.1 | Intron | XP_011522770.1 | ||||
XM_011524469.1 | Intron | XP_011522771.1 | ||||
XM_011524470.2 | Intron | XP_011522772.1 | ||||
XM_011524471.1 | Intron | XP_011522773.1 | ||||
XM_011524472.2 | Intron | XP_011522774.1 | ||||
XM_011524473.2 | Intron | XP_011522775.1 | ||||
XM_011524474.1 | Intron | XP_011522776.1 | ||||
XM_017024311.1 | Intron | XP_016879800.1 | ||||
XM_017024312.1 | Intron | XP_016879801.1 | ||||
XM_017024313.1 | Intron | XP_016879802.1 |