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CTCCTATCCTGTCAGCCGCAGTCGT[A/G]CTGCCAGCTCCAGCGAGGAGGAAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ARHGEF17 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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ARHGEF17 - Rho guanine nucleotide exchange factor 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014786.3 | 760 | Missense Mutation | ACT,GCT | T,A 247 | NP_055601.2 | |
XM_017018623.1 | 760 | Intron | XP_016874112.1 | |||
XM_017018624.1 | 760 | Intron | XP_016874113.1 |