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AGCTGCACATGTATTTATCATACAC[C/T]TTCCCTCTTCTGTCAGCTTCATCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 603134 MIM: 601573 | ||||||||||||||||||||
Literature Links: |
CUL1 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 |
CUL1 - cullin 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
EZH2 - enhancer of zeste 2 polycomb repressive complex 2 subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001203247.1 | 4502 | Silent Mutation | AAA,AAG | K,K 656 | NP_001190176.1 | |
NM_001203248.1 | 4502 | Silent Mutation | AAA,AAG | K,K 647 | NP_001190177.1 | |
NM_001203249.1 | 4502 | Silent Mutation | AAA,AAG | K,K 605 | NP_001190178.1 | |
NM_004456.4 | 4502 | Silent Mutation | AAA,AAG | K,K 661 | NP_004447.2 | |
NM_152998.2 | 4502 | Silent Mutation | AAA,AAG | K,K 617 | NP_694543.1 | |
XM_005249962.4 | 4502 | Silent Mutation | AAA,AAG | K,K 664 | XP_005250019.1 | |
XM_005249963.4 | 4502 | Silent Mutation | AAA,AAG | K,K 655 | XP_005250020.1 | |
XM_005249964.4 | 4502 | Silent Mutation | AAA,AAG | K,K 613 | XP_005250021.1 | |
XM_011515883.2 | 4502 | Silent Mutation | AAA,AAG | K,K 669 | XP_011514185.1 | |
XM_011515884.2 | 4502 | Silent Mutation | AAA,AAG | K,K 661 | XP_011514186.1 | |
XM_011515885.2 | 4502 | Silent Mutation | AAA,AAG | K,K 660 | XP_011514187.1 | |
XM_011515886.2 | 4502 | Silent Mutation | AAA,AAG | K,K 653 | XP_011514188.1 | |
XM_011515887.2 | 4502 | Silent Mutation | AAA,AAG | K,K 652 | XP_011514189.1 | |
XM_011515888.2 | 4502 | Silent Mutation | AAA,AAG | K,K 652 | XP_011514190.1 | |
XM_011515889.2 | 4502 | Silent Mutation | AAA,AAG | K,K 639 | XP_011514191.1 | |
XM_011515890.2 | 4502 | Silent Mutation | AAA,AAG | K,K 630 | XP_011514192.1 | |
XM_011515891.2 | 4502 | Silent Mutation | AAA,AAG | K,K 628 | XP_011514193.1 | |
XM_011515892.2 | 4502 | Silent Mutation | AAA,AAG | K,K 627 | XP_011514194.1 | |
XM_011515893.2 | 4502 | Silent Mutation | AAA,AAG | K,K 625 | XP_011514195.1 | |
XM_011515894.2 | 4502 | Silent Mutation | AAA,AAG | K,K 622 | XP_011514196.1 | |
XM_011515895.2 | 4502 | Silent Mutation | AAA,AAG | K,K 621 | XP_011514197.1 | |
XM_011515896.2 | 4502 | Silent Mutation | AAA,AAG | K,K 583 | XP_011514198.1 | |
XM_011515897.2 | 4502 | Silent Mutation | AAA,AAG | K,K 552 | XP_011514199.1 | |
XM_011515898.2 | 4502 | Silent Mutation | AAA,AAG | K,K 552 | XP_011514200.1 | |
XM_011515899.2 | 4502 | Intron | XP_011514201.1 | |||
XM_011515901.2 | 4502 | Intron | XP_011514203.1 | |||
XM_017011817.1 | 4502 | Silent Mutation | AAA,AAG | K,K 669 | XP_016867306.1 | |
XM_017011818.1 | 4502 | Silent Mutation | AAA,AAG | K,K 648 | XP_016867307.1 | |
XM_017011819.1 | 4502 | Silent Mutation | AAA,AAG | K,K 622 | XP_016867308.1 | |
XM_017011820.1 | 4502 | Silent Mutation | AAA,AAG | K,K 613 | XP_016867309.1 | |
XM_017011821.1 | 4502 | Silent Mutation | AAA,AAG | K,K 547 | XP_016867310.1 |