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CGGAGCCCGCGCACGTCCCAGAGGC[A/G]CAGGGCGCCGTCGTGCGAGGCGGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607981 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NUB1 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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NUB1 - negative regulator of ubiquitin like proteins 1 | ||||||
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There are no transcripts associated with this gene. |
WDR86 - WD repeat domain 86 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001284260.1 | 1458 | Missense Mutation | GCG,GTG | A,V 359 | NP_001271189.1 | |
NM_001284261.1 | 1458 | Silent Mutation | TGC,TGT | C,C 164 | NP_001271190.1 | |
NM_001284262.1 | 1458 | Missense Mutation | CGC,TGC | R,C 210 | NP_001271191.1 | |
NM_198285.2 | 1458 | Missense Mutation | CGC,TGC | R,C 338 | NP_938026.2 | |
XM_005249989.3 | 1458 | Silent Mutation | TGC,TGT | C,C 292 | XP_005250046.1 | |
XM_005249990.4 | 1458 | Intron | XP_005250047.1 | |||
XM_006715966.2 | 1458 | Intron | XP_006716029.1 | |||
XM_011516144.2 | 1458 | Missense Mutation | GCG,GTG | A,V 359 | XP_011514446.1 | |
XM_011516145.2 | 1458 | Intron | XP_011514447.1 | |||
XM_011516146.2 | 1458 | Missense Mutation | CGC,TGC | R,C 338 | XP_011514448.1 | |
XM_011516147.2 | 1458 | Silent Mutation | TGC,TGT | C,C 292 | XP_011514449.1 | |
XM_011516148.1 | 1458 | Missense Mutation | GCG,GTG | A,V 231 | XP_011514450.1 | |
XM_011516150.1 | 1458 | Missense Mutation | GCG,GTG | A,V 231 | XP_011514452.1 | |
XM_011516151.2 | 1458 | Intron | XP_011514453.1 | |||
XM_011516152.1 | 1458 | Intron | XP_011514454.1 |