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TTTTCTCCCAACTGTTCCTTTTTTT[A/T]AAAAAAGTATTGTTTTAGACAGTAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 116946 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDC27 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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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
|
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AMR
|
CDC27 - cell division cycle 27 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114091.2 | 4248 | Intron | NP_001107563.1 | |||
NM_001256.4 | 4248 | Intron | NP_001247.3 | |||
NM_001293089.1 | 4248 | Intron | NP_001280018.1 | |||
NM_001293091.1 | 4248 | Intron | NP_001280020.1 | |||
XM_011525546.2 | 4248 | UTR 3 | XP_011523848.1 | |||
XM_011525547.2 | 4248 | UTR 3 | XP_011523849.1 | |||
XM_011525548.2 | 4248 | UTR 3 | XP_011523850.1 | |||
XM_011525549.2 | 4248 | UTR 3 | XP_011523851.1 | |||
XM_011525550.2 | 4248 | UTR 3 | XP_011523852.1 | |||
XM_017025481.1 | 4248 | Intron | XP_016880970.1 | |||
XM_017025482.1 | 4248 | UTR 3 | XP_016880971.1 | |||
XM_017025483.1 | 4248 | UTR 3 | XP_016880972.1 | |||
XM_017025484.1 | 4248 | UTR 3 | XP_016880973.1 | |||
XM_017025485.1 | 4248 | UTR 3 | XP_016880974.1 | |||
XM_017025486.1 | 4248 | UTR 3 | XP_016880975.1 | |||
XM_017025487.1 | 4248 | UTR 3 | XP_016880976.1 | |||
XM_017025488.1 | 4248 | UTR 3 | XP_016880977.1 |