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GGCAACTGTCTGATTAGGTCCTTAA[C/T]AGCAGCGACTCGCTGTCTTGGTTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610577 | ||||||||||||||||||||
Literature Links: |
ARHGAP12 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ARHGAP12 - Rho GTPase activating protein 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270695.1 | 2375 | Missense Mutation | ATT,GTT | I,V 760 | NP_001257624.1 | |
NM_001270696.1 | 2375 | Missense Mutation | ATT,GTT | I,V 735 | NP_001257625.1 | |
NM_001270697.1 | 2375 | Missense Mutation | ATT,GTT | I,V 718 | NP_001257626.1 | |
NM_001270698.1 | 2375 | Missense Mutation | ATT,GTT | I,V 688 | NP_001257627.1 | |
NM_001270699.1 | 2375 | Missense Mutation | ATT,GTT | I,V 713 | NP_001257628.1 | |
NM_018287.6 | 2375 | Missense Mutation | ATT,GTT | I,V 765 | NP_060757.4 | |
XM_005252644.1 | 2375 | Missense Mutation | ATT,GTT | I,V 713 | XP_005252701.1 | |
XM_011519761.1 | 2375 | Missense Mutation | ATT,GTT | I,V 691 | XP_011518063.1 | |
XM_017016954.1 | 2375 | Missense Mutation | ATT,GTT | I,V 661 | XP_016872443.1 |