Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607489 MIM: 600589 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CUL9 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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CUL9 - cullin 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015089.3 | 1261 | Missense Mutation | CGG,GGG | R,G 156 | NP_055904.1 | |
XM_011514422.1 | 1261 | Missense Mutation | CGG,GGG | R,G 156 | XP_011512724.1 | |
XM_011514423.2 | 1261 | Missense Mutation | CGG,GGG | R,G 156 | XP_011512725.1 | |
XM_011514424.1 | 1261 | Missense Mutation | CGG,GGG | R,G 156 | XP_011512726.1 | |
XM_011514425.1 | 1261 | Missense Mutation | CGG,GGG | R,G 156 | XP_011512727.1 | |
XM_011514426.1 | 1261 | Missense Mutation | CGG,GGG | R,G 156 | XP_011512728.1 | |
XM_011514427.1 | 1261 | Intron | XP_011512729.1 | |||
XM_011514428.1 | 1261 | Missense Mutation | CGG,GGG | R,G 156 | XP_011512730.1 | |
XM_011514429.1 | 1261 | Intron | XP_011512731.1 | |||
XM_011514430.1 | 1261 | Missense Mutation | CGG,GGG | R,G 156 | XP_011512732.1 | |
XM_017010589.1 | 1261 | Missense Mutation | CGG,GGG | R,G 156 | XP_016866078.1 | |
XM_017010590.1 | 1261 | Intron | XP_016866079.1 |
SRF - serum response factor | ||||||
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There are no transcripts associated with this gene. |