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TCCACGGGGGTCAGGAACTCGTACT[C/T]CTCGGCCCGGGGCCCATAGCTGCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601925 MIM: 176790 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGDIA 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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ARHGDIA - Rho GDP dissociation inhibitor alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001185077.2 | 959 | Missense Mutation | AAG,GAG | K,E 155 | NP_001172006.1 | |
NM_001185078.2 | 959 | Intron | NP_001172007.1 | |||
NM_001301240.1 | 959 | Missense Mutation | AAG,GAG | K,E 155 | NP_001288169.1 | |
NM_001301241.1 | 959 | Missense Mutation | AAG,GAG | K,E 155 | NP_001288170.1 | |
NM_001301242.1 | 959 | Intron | NP_001288171.1 | |||
NM_001301243.1 | 959 | Missense Mutation | AAG,GAG | K,E 200 | NP_001288172.1 | |
NM_004309.5 | 959 | Missense Mutation | AAG,GAG | K,E 155 | NP_004300.1 | |
XM_011523574.1 | 959 | Missense Mutation | AAG,GAG | K,E 200 | XP_011521876.1 |
P4HB - prolyl 4-hydroxylase subunit beta | ||||||
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There are no transcripts associated with this gene. |