Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGACCCCATTTAGACACTCACATT[C/T]GGGGGCCCCTCTCTGAGGAGAATTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 157680 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDC25C PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
CDC25C - cell division cycle 25C | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287582.1 | 1591 | Missense Mutation | CAA,CGA | Q,R 386 | NP_001274511.1 | |
NM_001287583.1 | 1591 | Missense Mutation | CAA,CGA | Q,R 464 | NP_001274512.1 | |
NM_001318098.1 | 1591 | Missense Mutation | CAA,CGA | Q,R 403 | NP_001305027.1 | |
NM_001790.4 | 1591 | Missense Mutation | CAA,CGA | Q,R 386 | NP_001781.2 | |
NM_022809.3 | 1591 | Missense Mutation | CAA,CGA | Q,R 313 | NP_073720.1 | |
XM_005272145.3 | 1591 | Missense Mutation | CAA,CGA | Q,R 430 | XP_005272202.1 | |
XM_006714739.3 | 1591 | Missense Mutation | CAA,CGA | Q,R 388 | XP_006714802.1 | |
XM_011543759.2 | 1591 | Missense Mutation | CAA,CGA | Q,R 410 | XP_011542061.1 | |
XM_011543760.2 | 1591 | Missense Mutation | CAA,CGA | Q,R 409 | XP_011542062.1 | |
XM_011543761.2 | 1591 | Missense Mutation | CAA,CGA | Q,R 391 | XP_011542063.1 | |
XM_011543762.1 | 1591 | Missense Mutation | CAA,CGA | Q,R 313 | XP_011542064.1 | |
XM_011543763.1 | 1591 | Missense Mutation | CAA,CGA | Q,R 275 | XP_011542065.1 | |
XM_011543764.1 | 1591 | Missense Mutation | CAA,CGA | Q,R 224 | XP_011542066.1 | |
XM_017010101.1 | 1591 | Missense Mutation | CAA,CGA | Q,R 352 | XP_016865590.1 |