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- SNP ID:
- rs11119836
- Gene
-
DTLINTS7 - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.1: 212037032 - 212037032 on Build GRCh38
- Polymorphism:
- C/G, Transversion substitution
- Context Sequence [VIC/FAM]:
TCTTTGTAATTATACTTAAATGCTC[C/G]TCTTTCTGTCTCTCCTGGGACCTTG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
34 submissions
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Phenotype: |
MIM: 610617
MIM: 611350
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Literature Links: |
DTL PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | ||||||
|---|---|---|---|---|---|---|---|---|
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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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| DTL - denticleless E3 ubiquitin protein ligase homolog | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001286229.1 | Intron | NP_001273158.1 | ||||
| NM_001286230.1 | Intron | NP_001273159.1 | ||||
| NM_016448.3 | Intron | NP_057532.3 | ||||
| XM_011509614.1 | Intron | XP_011507916.1 | ||||
| INTS7 - integrator complex subunit 7 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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HapMap