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GGGATGAGCACCAGCTCCACCACGC[C/G]TGGGGCGCACTGCGCGATCTTGCGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 116949 MIM: 117140 MIM: 610674 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDC25B 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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CDC25B - cell division cycle 25B | ||||||
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There are no transcripts associated with this gene. |
CENPB - centromere protein B | ||||||
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There are no transcripts associated with this gene. |
SPEF1 - sperm flagellar 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015417.4 | 471 | Missense Mutation | CGC,GGC | R,G 98 | NP_056232.2 | |
XM_005260683.4 | 471 | Missense Mutation | CGC,GGC | R,G 98 | XP_005260740.1 |