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TGCACTTTCTTTTCTAGGAGAGAGA[C/T]TGATGACTTTTTTAAAGCAGATGAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 613421 MIM: 608047 | ||||||||||||||||||||
Literature Links: |
KCTD10 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 |
KCTD10 - potassium channel tetramerization domain containing 10 | ||||||
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There are no transcripts associated with this gene. |
UBE3B - ubiquitin protein ligase E3B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270449.1 | 439 | Missense Mutation | ACT,ATT | T,I 57 | NP_001257378.1 | |
NM_001270450.1 | 439 | Missense Mutation | ACT,ATT | T,I 57 | NP_001257379.1 | |
NM_001270451.1 | 439 | Missense Mutation | ACT,ATT | T,I 57 | NP_001257380.1 | |
NM_130466.3 | 439 | Missense Mutation | ACT,ATT | T,I 57 | NP_569733.2 | |
NM_183415.2 | 439 | Missense Mutation | ACT,ATT | T,I 57 | NP_904324.1 | |
XM_005253987.2 | 439 | Missense Mutation | ACT,ATT | T,I 57 | XP_005254044.1 | |
XM_006719681.3 | 439 | Missense Mutation | ACT,ATT | T,I 57 | XP_006719744.1 | |
XM_006719682.2 | 439 | Missense Mutation | ACT,ATT | T,I 57 | XP_006719745.1 | |
XM_011538959.2 | 439 | Missense Mutation | ACT,ATT | T,I 57 | XP_011537261.1 | |
XM_011538961.1 | 439 | Missense Mutation | ACT,ATT | T,I 57 | XP_011537263.1 | |
XM_017020195.1 | 439 | UTR 5 | XP_016875684.1 | |||
XM_017020196.1 | 439 | Missense Mutation | ACT,ATT | T,I 57 | XP_016875685.1 |