Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
41 submissions
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Phenotype: |
MIM: 116900 MIM: 606903 MIM: 600560 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CKS1B 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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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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CKS1B - CDC28 protein kinase regulatory subunit 1B | ||||||
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There are no transcripts associated with this gene. |
LOC101928120 - uncharacterized LOC101928120 | ||||||
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There are no transcripts associated with this gene. |
MIR4258 - microRNA 4258 | ||||||
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There are no transcripts associated with this gene. |
PBXIP1 - PBX homeobox interacting protein 1 | ||||||
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There are no transcripts associated with this gene. |
PYGO2 - pygopus family PHD finger 2 | ||||||
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There are no transcripts associated with this gene. |
SHC1 - SHC adaptor protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130040.1 | 1157 | Intron | NP_001123512.1 | |||
NM_001130041.1 | 1157 | Intron | NP_001123513.1 | |||
NM_001202859.1 | 1157 | Intron | NP_001189788.1 | |||
NM_003029.4 | 1157 | Intron | NP_003020.2 | |||
NM_183001.4 | 1157 | Intron | NP_892113.4 | |||
XM_005245449.4 | 1157 | Silent Mutation | CGC,CGG | R,R 469 | XP_005245506.1 | |
XM_005245451.4 | 1157 | Silent Mutation | CGC,CGG | R,R 359 | XP_005245508.1 | |
XM_011509892.2 | 1157 | Silent Mutation | CGC,CGG | R,R 479 | XP_011508194.1 | |
XM_011509893.2 | 1157 | Silent Mutation | CGC,CGG | R,R 478 | XP_011508195.1 | |
XM_011509894.2 | 1157 | Silent Mutation | CGC,CGG | R,R 461 | XP_011508196.1 | |
XM_011509897.1 | 1157 | Intron | XP_011508199.1 | |||
XM_011509898.2 | 1157 | Silent Mutation | CGC,CGG | R,R 303 | XP_011508200.1 | |
XM_017002081.1 | 1157 | Silent Mutation | CGC,CGG | R,R 452 | XP_016857570.1 | |
XM_017002082.1 | 1157 | Silent Mutation | CGC,CGG | R,R 451 | XP_016857571.1 | |
XM_017002083.1 | 1157 | Intron | XP_016857572.1 |
Set Membership: |
HapMap |