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GAAGGGGGATTCCTTCGAAGAGGTG[A/G]TCGTGGAGGGCGGGGCAGCAGAGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 157680 MIM: 609372 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDC25C 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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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 | 292 | Intron | NP_001274511.1 | |||
NM_001287583.1 | 292 | Intron | NP_001274512.1 | |||
NM_001318098.1 | 292 | Intron | NP_001305027.1 | |||
NM_001790.4 | 292 | Intron | NP_001781.2 | |||
NM_022809.3 | 292 | Intron | NP_073720.1 | |||
XM_005272145.3 | 292 | Intron | XP_005272202.1 | |||
XM_006714739.3 | 292 | Intron | XP_006714802.1 | |||
XM_011543759.2 | 292 | Intron | XP_011542061.1 | |||
XM_011543760.2 | 292 | Intron | XP_011542062.1 | |||
XM_011543761.2 | 292 | Intron | XP_011542063.1 | |||
XM_011543762.1 | 292 | Intron | XP_011542064.1 | |||
XM_011543763.1 | 292 | Intron | XP_011542065.1 | |||
XM_011543764.1 | 292 | Intron | XP_011542066.1 | |||
XM_017010101.1 | 292 | Intron | XP_016865590.1 |
FAM53C - family with sequence similarity 53 member C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135647.1 | 292 | UTR 5 | NP_001129119.1 | |||
NM_016605.2 | 292 | Intron | NP_057689.1 |