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TTTGACAGTGAAAGGGCTGATGGAA[C/T]TATATCATCTGAGATAAAATCAGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 116901 MIM: 607693 | ||||||||||||||||||||
Literature Links: |
CKS2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CKS2 - CDC28 protein kinase regulatory subunit 2 | ||||||
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There are no transcripts associated with this gene. |
SECISBP2 - SECIS binding protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282688.1 | 658 | Missense Mutation | ACT,ATT | T,I 166 | NP_001269617.1 | |
NM_001282689.1 | 658 | Missense Mutation | ACT,ATT | T,I 94 | NP_001269618.1 | |
NM_001282690.1 | 658 | Missense Mutation | ACT,ATT | T,I 99 | NP_001269619.1 | |
NM_024077.4 | 658 | Missense Mutation | ACT,ATT | T,I 167 | NP_076982.3 | |
XM_005252196.2 | 658 | Missense Mutation | ACT,ATT | T,I 167 | XP_005252253.1 | |
XM_005252202.3 | 658 | Intron | XP_005252259.1 | |||
XM_006717282.2 | 658 | Missense Mutation | ACT,ATT | T,I 94 | XP_006717345.1 | |
XM_011519000.2 | 658 | Missense Mutation | ACT,ATT | T,I 99 | XP_011517302.1 | |
XM_011519001.1 | 658 | Missense Mutation | ACT,ATT | T,I 99 | XP_011517303.1 | |
XM_011519002.1 | 658 | Missense Mutation | ACT,ATT | T,I 99 | XP_011517304.1 | |
XM_011519003.1 | 658 | Missense Mutation | ACT,ATT | T,I 99 | XP_011517305.1 | |
XM_017015122.1 | 658 | Missense Mutation | ACT,ATT | T,I 167 | XP_016870611.1 | |
XM_017015123.1 | 658 | Missense Mutation | ACT,ATT | T,I 167 | XP_016870612.1 | |
XM_017015124.1 | 658 | Missense Mutation | ACT,ATT | T,I 167 | XP_016870613.1 | |
XM_017015125.1 | 658 | UTR 5 | XP_016870614.1 |