Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCAAGTGCTTCTCATTGGAGGTGA[A/T]CTGCAAGGGCAGGAGGAAGAAGACA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 116806 MIM: 617010 | ||||||||||||||||||||
Literature Links: |
CTNNB1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
CTNNB1 - catenin beta 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
ULK4 - unc-51 like kinase 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001322500.1 | 4646 | Intron | NP_001309429.1 | |||
NM_001322501.1 | 4646 | Missense Mutation | ATC,TTC | I,F 925 | NP_001309430.1 | |
NM_017886.3 | 4646 | Missense Mutation | ATC,TTC | I,F 1227 | NP_060356.2 | |
XM_011533874.2 | 4646 | Intron | XP_011532176.1 | |||
XM_011533880.2 | 4646 | Missense Mutation | ATC,TTC | I,F 618 | XP_011532182.1 | |
XM_017006711.1 | 4646 | Missense Mutation | ATC,TTC | I,F 1199 | XP_016862200.1 | |
XM_017006712.1 | 4646 | Intron | XP_016862201.1 |