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CAGACTGCGCGTCGAAGGCCCGGGC[A/G]CAAGCGTCCCCGCTGCCCGTGAACA
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 |
---|---|---|
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 |
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 | 1334 | Missense Mutation | NP_001271189.1 | |||
NM_001284261.1 | 1334 | Missense Mutation | NP_001271190.1 | |||
NM_001284262.1 | 1334 | Silent Mutation | NP_001271191.1 | |||
NM_198285.2 | 1334 | Silent Mutation | NP_938026.2 | |||
XM_005249989.3 | 1334 | Missense Mutation | XP_005250046.1 | |||
XM_005249990.4 | 1334 | Silent Mutation | XP_005250047.1 | |||
XM_006715966.2 | 1334 | Intron | XP_006716029.1 | |||
XM_011516144.2 | 1334 | Missense Mutation | XP_011514446.1 | |||
XM_011516145.2 | 1334 | Missense Mutation | XP_011514447.1 | |||
XM_011516146.2 | 1334 | Silent Mutation | XP_011514448.1 | |||
XM_011516147.2 | 1334 | Missense Mutation | XP_011514449.1 | |||
XM_011516148.1 | 1334 | Missense Mutation | XP_011514450.1 | |||
XM_011516150.1 | 1334 | Missense Mutation | XP_011514452.1 | |||
XM_011516151.2 | 1334 | Missense Mutation | XP_011514453.1 | |||
XM_011516152.1 | 1334 | Intron | XP_011514454.1 |