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AGAAATTTGGTGTATTTAATTCTGG[G/T]ACTGTCATTTTTGTCTGTTCAAGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
41 submissions
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Phenotype: |
MIM: 603311 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDC7 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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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CDC7 - cell division cycle 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001134419.1 | Intron | NP_001127891.1 | ||||
NM_001134420.1 | Intron | NP_001127892.1 | ||||
NM_003503.3 | Intron | NP_003494.1 | ||||
XM_005271241.2 | Intron | XP_005271298.1 | ||||
XM_005271244.2 | Intron | XP_005271301.1 | ||||
XM_017002425.1 | Intron | XP_016857914.1 | ||||
XM_017002426.1 | Intron | XP_016857915.1 | ||||
XM_017002427.1 | Intron | XP_016857916.1 |