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GCTGGCAGGGAGTTGGCGCTGCTCA[A/G]TTTTTTCTGCGTGACCTGCTGCTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300118 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGAP6 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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ARHGAP6 - Rho GTPase activating protein 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287242.1 | 2426 | Silent Mutation | CTG,TTG | L,L 746 | NP_001274171.1 | |
NM_006125.2 | 2426 | Intron | NP_006116.2 | |||
NM_013423.2 | 2426 | Silent Mutation | CTG,TTG | L,L 723 | NP_038267.1 | |
NM_013427.2 | 2426 | Silent Mutation | CTG,TTG | L,L 926 | NP_038286.2 |