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AGCTATGGCGAGCCCTGCTGTCTCC[C/G]GCCCCTCCCCAGTCAGGGGGCCCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610576 MIM: 165220 MIM: 612031 | ||||||||||||||||||||
Literature Links: |
ARHGAP9 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 |
ARHGAP9 - Rho GTPase activating protein 9 | ||||||
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There are no transcripts associated with this gene. |
GLI1 - GLI family zinc finger 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001160045.1 | 383 | Intron | NP_001153517.1 | |||
NM_001167609.1 | 383 | Missense Mutation | CCG,CGG | P,R 20 | NP_001161081.1 | |
NM_005269.2 | 383 | Missense Mutation | CCG,CGG | P,R 20 | NP_005260.1 | |
XM_011538189.2 | 383 | Missense Mutation | CCG,CGG | P,R 20 | XP_011536491.1 | |
XM_011538190.1 | 383 | Missense Mutation | CCG,CGG | P,R 20 | XP_011536492.1 |
INHBE - inhibin beta E subunit | ||||||
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There are no transcripts associated with this gene. |