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ACTGTTCACTGATTTGAGCTGTAAT[A/C]CAGAAATGATGAAGAATGCAGCAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
24 submissions
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Phenotype: |
MIM: 612375 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
AIDA 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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AIDA - axin interactor, dorsalization associated | ||||||
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There are no transcripts associated with this gene. |
BROX - BRO1 domain and CAAX motif containing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288579.1 | 635 | Missense Mutation | ACA,CCA | T,P 54 | NP_001275508.1 | |
NM_001288580.1 | 635 | Missense Mutation | ACA,CCA | T,P 54 | NP_001275509.1 | |
NM_001288581.1 | 635 | Missense Mutation | ACA,CCA | T,P 54 | NP_001275510.1 | |
NM_144695.3 | 635 | Missense Mutation | ACA,CCA | T,P 54 | NP_653296.2 | |
XM_005273065.2 | 635 | Missense Mutation | ACA,CCA | T,P 54 | XP_005273122.2 | |
XM_005273069.4 | 635 | UTR 5 | XP_005273126.1 | |||
XM_006711173.3 | 635 | Missense Mutation | ACA,CCA | T,P 71 | XP_006711236.1 | |
XM_011509212.2 | 635 | Missense Mutation | ACA,CCA | T,P 107 | XP_011507514.1 | |
XM_011509213.2 | 635 | Missense Mutation | ACA,CCA | T,P 68 | XP_011507515.1 | |
XM_011509214.2 | 635 | Missense Mutation | ACA,CCA | T,P 54 | XP_011507516.1 | |
XM_017000374.1 | 635 | Missense Mutation | ACA,CCA | T,P 54 | XP_016855863.1 | |
XM_017000375.1 | 635 | Missense Mutation | ACA,CCA | T,P 68 | XP_016855864.1 | |
XM_017000376.1 | 635 | UTR 5 | XP_016855865.1 |