Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTCCTTCACCAGAAGGGCAATCTGC[C/T]CCCGCAGCTGCCGCTCCCCTTCCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 157680 | ||||||||||||||||||||
Literature Links: |
CDC25C 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 |
CDC25C - cell division cycle 25C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287582.1 | 1819 | Missense Mutation | GAG,GGG | E,G 462 | NP_001274511.1 | |
NM_001287583.1 | 1819 | Missense Mutation | GAG,GGG | E,G 540 | NP_001274512.1 | |
NM_001318098.1 | 1819 | Missense Mutation | GAG,GGG | E,G 479 | NP_001305027.1 | |
NM_001790.4 | 1819 | Missense Mutation | GAG,GGG | E,G 462 | NP_001781.2 | |
NM_022809.3 | 1819 | Missense Mutation | GAG,GGG | E,G 389 | NP_073720.1 | |
XM_005272145.3 | 1819 | Missense Mutation | GAG,GGG | E,G 506 | XP_005272202.1 | |
XM_006714739.3 | 1819 | Missense Mutation | GAG,GGG | E,G 464 | XP_006714802.1 | |
XM_011543759.2 | 1819 | Missense Mutation | GAG,GGG | E,G 486 | XP_011542061.1 | |
XM_011543760.2 | 1819 | Missense Mutation | GAG,GGG | E,G 485 | XP_011542062.1 | |
XM_011543761.2 | 1819 | Missense Mutation | GAG,GGG | E,G 467 | XP_011542063.1 | |
XM_011543762.1 | 1819 | Missense Mutation | GAG,GGG | E,G 389 | XP_011542064.1 | |
XM_011543763.1 | 1819 | Missense Mutation | GAG,GGG | E,G 351 | XP_011542065.1 | |
XM_011543764.1 | 1819 | Missense Mutation | GAG,GGG | E,G 300 | XP_011542066.1 | |
XM_017010101.1 | 1819 | Missense Mutation | GAG,GGG | E,G 428 | XP_016865590.1 |