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- SNP ID:
- rs373975096
- Gene
-
CUL1EZH2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.7: 148807670 - 148807670 on Build GRCh38
- Polymorphism:
- G/A, Transition substitution
- Context Sequence [VIC/FAM]:
GTCAAGGGATTTCCATTTCTCTTTC[G/A]ATGCCGACATACTTCAGGGCATCAG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 603134
MIM: 601573
|
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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 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001203247.1 | 4751 | Silent Mutation | ATC,ATT | I,I 739 | NP_001190176.1 | |
| NM_001203248.1 | 4751 | Silent Mutation | ATC,ATT | I,I 730 | NP_001190177.1 | |
| NM_001203249.1 | 4751 | Silent Mutation | ATC,ATT | I,I 688 | NP_001190178.1 | |
| NM_004456.4 | 4751 | Silent Mutation | ATC,ATT | I,I 744 | NP_004447.2 | |
| NM_152998.2 | 4751 | Silent Mutation | ATC,ATT | I,I 700 | NP_694543.1 | |
| XM_005249962.4 | 4751 | Silent Mutation | ATC,ATT | I,I 747 | XP_005250019.1 | |
| XM_005249963.4 | 4751 | Silent Mutation | ATC,ATT | I,I 738 | XP_005250020.1 | |
| XM_005249964.4 | 4751 | Silent Mutation | ATC,ATT | I,I 696 | XP_005250021.1 | |
| XM_011515883.2 | 4751 | Silent Mutation | ATC,ATT | I,I 752 | XP_011514185.1 | |
| XM_011515884.2 | 4751 | Silent Mutation | ATC,ATT | I,I 744 | XP_011514186.1 | |
| XM_011515885.2 | 4751 | Silent Mutation | ATC,ATT | I,I 743 | XP_011514187.1 | |
| XM_011515886.2 | 4751 | Silent Mutation | ATC,ATT | I,I 736 | XP_011514188.1 | |
| XM_011515887.2 | 4751 | Silent Mutation | ATC,ATT | I,I 735 | XP_011514189.1 | |
| XM_011515888.2 | 4751 | Silent Mutation | ATC,ATT | I,I 735 | XP_011514190.1 | |
| XM_011515889.2 | 4751 | Silent Mutation | ATC,ATT | I,I 722 | XP_011514191.1 | |
| XM_011515890.2 | 4751 | Silent Mutation | ATC,ATT | I,I 713 | XP_011514192.1 | |
| XM_011515891.2 | 4751 | Silent Mutation | ATC,ATT | I,I 711 | XP_011514193.1 | |
| XM_011515892.2 | 4751 | Silent Mutation | ATC,ATT | I,I 710 | XP_011514194.1 | |
| XM_011515893.2 | 4751 | Silent Mutation | ATC,ATT | I,I 708 | XP_011514195.1 | |
| XM_011515894.2 | 4751 | Silent Mutation | ATC,ATT | I,I 705 | XP_011514196.1 | |
| XM_011515895.2 | 4751 | Silent Mutation | ATC,ATT | I,I 704 | XP_011514197.1 | |
| XM_011515896.2 | 4751 | Silent Mutation | ATC,ATT | I,I 666 | XP_011514198.1 | |
| XM_011515897.2 | 4751 | Silent Mutation | ATC,ATT | I,I 635 | XP_011514199.1 | |
| XM_011515898.2 | 4751 | Silent Mutation | ATC,ATT | I,I 635 | XP_011514200.1 | |
| XM_011515899.2 | 4751 | Intron | XP_011514201.1 | |||
| XM_011515901.2 | 4751 | Intron | XP_011514203.1 | |||
| XM_017011817.1 | 4751 | Silent Mutation | ATC,ATT | I,I 752 | XP_016867306.1 | |
| XM_017011818.1 | 4751 | Silent Mutation | ATC,ATT | I,I 731 | XP_016867307.1 | |
| XM_017011819.1 | 4751 | Silent Mutation | ATC,ATT | I,I 705 | XP_016867308.1 | |
| XM_017011820.1 | 4751 | Silent Mutation | ATC,ATT | I,I 696 | XP_016867309.1 | |
| XM_017011821.1 | 4751 | Silent Mutation | ATC,ATT | I,I 630 | XP_016867310.1 | |
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