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TCCAGGACTTCCTCTCCAGGGCAGT[C/G]ATGGGAACAAGAGATTCTTAAGTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
6 submissions
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Phenotype: |
MIM: 612494 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGEF10L 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
|
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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ARHGEF10L - Rho guanine nucleotide exchange factor 10 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001011722.2 | Intron | NP_001011722.2 | ||||
NM_001319837.1 | Intron | NP_001306766.1 | ||||
NM_001319838.1 | Intron | NP_001306767.1 | ||||
NM_001328124.1 | Intron | NP_001315053.1 | ||||
NM_018125.3 | Intron | NP_060595.3 | ||||
XM_005245923.2 | Intron | XP_005245980.2 | ||||
XM_005245925.2 | Intron | XP_005245982.2 | ||||
XM_005245927.2 | Intron | XP_005245984.2 | ||||
XM_005245929.2 | Intron | XP_005245986.2 | ||||
XM_006710728.1 | Intron | XP_006710791.1 | ||||
XM_006710729.1 | Intron | XP_006710792.1 | ||||
XM_006710731.1 | Intron | XP_006710794.1 | ||||
XM_011541691.2 | Intron | XP_011539993.1 | ||||
XM_011541692.2 | Intron | XP_011539994.1 | ||||
XM_011541693.2 | Intron | XP_011539995.1 | ||||
XM_011541695.2 | Intron | XP_011539997.1 | ||||
XM_011541696.2 | Intron | XP_011539998.1 | ||||
XM_017001617.1 | Intron | XP_016857106.1 | ||||
XM_017001618.1 | Intron | XP_016857107.1 | ||||
XM_017001619.1 | Intron | XP_016857108.1 | ||||
XM_017001620.1 | Intron | XP_016857109.1 | ||||
XM_017001621.1 | Intron | XP_016857110.1 | ||||
XM_017001622.1 | Intron | XP_016857111.1 |