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CTTGTTTGTGAAAAACTATAGGGAT[A/C]ATTTGTGTCTCTTTATGGTGTCATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616432 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGEF18 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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ARHGEF18 - Rho/Rac guanine nucleotide exchange factor 18 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130955.1 | Intron | NP_001124427.1 | ||||
NM_015318.3 | Intron | NP_056133.2 | ||||
XM_005272464.4 | Intron | XP_005272521.1 | ||||
XM_006722705.3 | Intron | XP_006722768.1 | ||||
XM_006722706.3 | Intron | XP_006722769.1 | ||||
XM_006722708.2 | Intron | XP_006722771.1 | ||||
XM_011527835.2 | Intron | XP_011526137.1 | ||||
XM_011527836.2 | Intron | XP_011526138.1 | ||||
XM_011527837.2 | Intron | XP_011526139.1 | ||||
XM_011527838.2 | Intron | XP_011526140.1 | ||||
XM_011527839.2 | Intron | XP_011526141.1 | ||||
XM_011527840.1 | Intron | XP_011526142.1 | ||||
XM_011527841.2 | Intron | XP_011526143.1 |