Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATCTGGAGCAGGCAGGTGGGGACG[C/G]CCATGCGGCTGATGCTGTCTGAGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612299 | ||||||||||||||||||||
Literature Links: |
COMMD9 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 |
COMMD9 - COMM domain containing 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001101653.1 | 430 | Missense Mutation | GCC,GGC | A,G 101 | NP_001095123.1 | |
NM_001307932.1 | 430 | Silent Mutation | GGC,GGG | G,G 131 | NP_001294861.1 | |
NM_001307937.1 | 430 | Missense Mutation | GCC,GGC | A,G 134 | NP_001294866.1 | |
NM_014186.3 | 430 | Missense Mutation | GCC,GGC | A,G 143 | NP_054905.2 | |
XM_017017625.1 | 430 | Intron | XP_016873114.1 |