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TCCTCAATGTCGCAGACCACTGTAG[A/G]CCCTGAGTCTGGGCTGGTCGCATCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609568 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGAP20 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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ARHGAP20 - Rho GTPase activating protein 20 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258415.1 | 3632 | Missense Mutation | CCT,TCT | P,S 1153 | NP_001245344.1 | |
NM_001258416.1 | 3632 | Missense Mutation | CCT,TCT | P,S 1150 | NP_001245345.1 | |
NM_001258417.1 | 3632 | Missense Mutation | CCT,TCT | P,S 1140 | NP_001245346.1 | |
NM_001258418.1 | 3632 | Missense Mutation | CCT,TCT | P,S 1140 | NP_001245347.1 | |
NM_020809.3 | 3632 | Missense Mutation | CCT,TCT | P,S 1176 | NP_065860.2 | |
XM_005271628.3 | 3632 | Missense Mutation | CCT,TCT | P,S 719 | XP_005271685.1 | |
XM_006718893.3 | 3632 | Missense Mutation | CCT,TCT | P,S 1176 | XP_006718956.1 |