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CCTGGTGAAGGGCGCCGTGGGGCTC[C/T]GCAGCCTCTGTCTCAGTTTCAGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616432 MIM: 607583 | ||||||||||||||||||||
Literature Links: |
ARHGEF18 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 |
ARHGEF18 - Rho/Rac guanine nucleotide exchange factor 18 | ||||||
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There are no transcripts associated with this gene. |
LOC100128573 - uncharacterized LOC100128573 | ||||||
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There are no transcripts associated with this gene. |
PEX11G - peroxisomal biogenesis factor 11 gamma | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270539.1 | 687 | Missense Mutation | CAG,CGG | Q,R 156 | NP_001257468.1 | |
NM_001300881.1 | 687 | Missense Mutation | CAG,CGG | Q,R 86 | NP_001287810.1 | |
NM_080662.3 | 687 | Missense Mutation | CAG,CGG | Q,R 156 | NP_542393.1 | |
XM_005272506.2 | 687 | Intron | XP_005272563.1 | |||
XM_011528426.2 | 687 | Intron | XP_011526728.1 | |||
XM_011528427.2 | 687 | Intron | XP_011526729.1 | |||
XM_011528428.1 | 687 | Missense Mutation | CAG,CGG | Q,R 86 | XP_011526730.1 | |
XM_011528429.2 | 687 | Missense Mutation | CAG,CGG | Q,R 86 | XP_011526731.1 | |
XM_011528431.2 | 687 | Missense Mutation | CAG,CGG | Q,R 86 | XP_011526733.1 | |
XM_011528432.1 | 687 | Intron | XP_011526734.1 |