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TCGTTTCATAGTTCAGTTCACTGTA[C/G]GGACGGGCAGCTGAGTAGAAGTCAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604275 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CTNND2 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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CTNND2 - catenin delta 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288715.1 | 3598 | Silent Mutation | CCC,CCG | P,P 1115 | NP_001275644.1 | |
NM_001288716.1 | 3598 | Silent Mutation | CCC,CCG | P,P 869 | NP_001275645.1 | |
NM_001288717.1 | 3598 | Silent Mutation | CCC,CCG | P,P 773 | NP_001275646.1 | |
NM_001332.3 | 3598 | Silent Mutation | CCC,CCG | P,P 1206 | NP_001323.1 | |
XM_005248251.3 | 3598 | Silent Mutation | CCC,CCG | P,P 1231 | XP_005248308.1 | |
XM_005248252.2 | 3598 | Silent Mutation | CCC,CCG | P,P 1217 | XP_005248309.1 | |
XM_005248253.1 | 3598 | Silent Mutation | CCC,CCG | P,P 1140 | XP_005248310.1 | |
XM_011513967.2 | 3598 | Silent Mutation | CCC,CCG | P,P 1140 | XP_011512269.1 | |
XM_017009072.1 | 3598 | Silent Mutation | CCC,CCG | P,P 985 | XP_016864561.1 | |
XM_017009073.1 | 3598 | Silent Mutation | CCC,CCG | P,P 971 | XP_016864562.1 | |
XM_017009074.1 | 3598 | Silent Mutation | CCC,CCG | P,P 960 | XP_016864563.1 | |
XM_017009075.1 | 3598 | Silent Mutation | CCC,CCG | P,P 894 | XP_016864564.1 | |
XM_017009076.1 | 3598 | Silent Mutation | CCC,CCG | P,P 894 | XP_016864565.1 |