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CAGGGGATAGGGGGAGGCTTCGGGG[A/C]CGTTCTGAGACCTGCAGGAGAAAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613991 | ||||||||||||||||||||
Literature Links: |
CDC42BPG PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CDC42BPG - CDC42 binding protein kinase gamma | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017525.2 | 4760 | Silent Mutation | CGG,CGT | R,R 1537 | NP_059995.2 | |
XM_011545155.2 | 4760 | Silent Mutation | CGG,CGT | R,R 1555 | XP_011543457.1 | |
XM_011545156.2 | 4760 | Silent Mutation | CGG,CGT | R,R 1548 | XP_011543458.1 | |
XM_011545157.2 | 4760 | Missense Mutation | GCC,TCC | A,S 1523 | XP_011543459.1 | |
XM_011545158.2 | 4760 | Silent Mutation | CGG,CGT | R,R 1481 | XP_011543460.1 | |
XM_011545159.2 | 4760 | Intron | XP_011543461.1 | |||
XM_011545160.2 | 4760 | Silent Mutation | CGG,CGT | R,R 1457 | XP_011543462.1 | |
XM_011545161.2 | 4760 | Intron | XP_011543463.1 | |||
XM_017017996.1 | 4760 | Silent Mutation | CGG,CGT | R,R 1554 | XP_016873485.1 | |
XM_017017997.1 | 4760 | Intron | XP_016873486.1 | |||
XM_017017998.1 | 4760 | Intron | XP_016873487.1 | |||
XM_017017999.1 | 4760 | Silent Mutation | CGG,CGT | R,R 851 | XP_016873488.1 |