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CGATGGAGCCACCGATGGAGCCGTC[C/T]GGAGGGGAGCAAGAGCCCGGAGCCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614142 MIM: 610287 MIM: 602327 | ||||||||||||||||||||
Literature Links: |
CUEDC2 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 |
CUEDC2 - CUE domain containing 2 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
FBXL15 - F-box and leucine rich repeat protein 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024326.3 | 1340 | Silent Mutation | TCC,TCT | S,S 8 | NP_077302.3 | |
XM_005270149.2 | 1340 | Silent Mutation | TCC,TCT | S,S 95 | XP_005270206.1 | |
XM_005270150.4 | 1340 | Silent Mutation | TCC,TCT | S,S 8 | XP_005270207.1 | |
XM_005270151.3 | 1340 | Silent Mutation | TCC,TCT | S,S 8 | XP_005270208.1 | |
XM_017016631.1 | 1340 | Silent Mutation | TCC,TCT | S,S 8 | XP_016872120.1 |
PSD - pleckstrin and Sec7 domain containing | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270965.1 | 1340 | Intron | NP_001257894.1 | |||
NM_001270966.1 | 1340 | Intron | NP_001257895.1 | |||
NM_002779.4 | 1340 | Intron | NP_002770.3 | |||
XM_011539968.1 | 1340 | Intron | XP_011538270.1 | |||
XM_011539969.2 | 1340 | Intron | XP_011538271.1 | |||
XM_017016433.1 | 1340 | Intron | XP_016871922.1 | |||
XM_017016434.1 | 1340 | Intron | XP_016871923.1 |