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ACAAAGAGGTTCTGTCTTCCTGACC[A/T]GCATAAATGCTCCAGGAGGTACCGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610576 MIM: 165220 | ||||||||||||||||||||
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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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080156.2 | 2498 | Missense Mutation | AGG,TGG | R,W 491 | NP_001073625.1 | |
NM_001080157.1 | 2498 | Intron | NP_001073626.1 | |||
NM_001319850.1 | 2498 | Missense Mutation | AGG,TGG | R,W 765 | NP_001306779.1 | |
NM_001319851.1 | 2498 | Missense Mutation | AGG,TGG | R,W 364 | NP_001306780.1 | |
NM_001319852.1 | 2498 | Missense Mutation | AGG,TGG | R,W 510 | NP_001306781.1 | |
NM_032496.3 | 2498 | Missense Mutation | AGG,TGG | R,W 675 | NP_115885.2 | |
XM_005269083.2 | 2498 | Missense Mutation | AGG,TGG | R,W 510 | XP_005269140.1 | |
XM_005269084.2 | 2498 | Missense Mutation | AGG,TGG | R,W 479 | XP_005269141.1 | |
XM_005269085.2 | 2498 | Missense Mutation | AGG,TGG | R,W 479 | XP_005269142.1 | |
XM_011538656.2 | 2498 | Missense Mutation | AGG,TGG | R,W 675 | XP_011536958.1 | |
XM_011538657.2 | 2498 | Missense Mutation | AGG,TGG | R,W 663 | XP_011536959.1 | |
XM_011538658.2 | 2498 | Missense Mutation | AGG,TGG | R,W 644 | XP_011536960.1 | |
XM_011538659.2 | 2498 | Intron | XP_011536961.1 | |||
XM_017019800.1 | 2498 | Missense Mutation | AGG,TGG | R,W 510 | XP_016875289.1 | |
XM_017019801.1 | 2498 | Missense Mutation | AGG,TGG | R,W 491 | XP_016875290.1 | |
XM_017019802.1 | 2498 | Missense Mutation | AGG,TGG | R,W 460 | XP_016875291.1 | |
XM_017019803.1 | 2498 | Intron | XP_016875292.1 | |||
XM_017019804.1 | 2498 | Intron | XP_016875293.1 |
GLI1 - GLI family zinc finger 1 | ||||||
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There are no transcripts associated with this gene. |