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CTGATTTCCCGGCCCTCCGCTCTCT[C/G]CTAGGCAGGCAGGGGCCTGAAGGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610018 MIM: 605272 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGEF40 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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ARHGEF40 - Rho guanine nucleotide exchange factor 40 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278529.1 | Intron | NP_001265458.1 | ||||
NM_001278530.1 | Intron | NP_001265459.1 | ||||
NM_018071.4 | Intron | NP_060541.3 | ||||
XM_005267844.2 | Intron | XP_005267901.1 | ||||
XM_011536937.2 | Intron | XP_011535239.1 | ||||
XM_011536938.2 | Intron | XP_011535240.1 | ||||
XM_017021434.1 | Intron | XP_016876923.1 | ||||
XM_017021435.1 | Intron | XP_016876924.1 | ||||
XM_017021436.1 | Intron | XP_016876925.1 | ||||
XM_017021437.1 | Intron | XP_016876926.1 |