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- SNP ID:
- rs761915039
- Gene
-
POLQ - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.3: 121463238 - 121463238 on Build GRCh38
- Polymorphism:
- T/G, Transversion substitution
- Context Sequence [VIC/FAM]:
ATGGTAGTGAGTCCGTCTCACGAGA[T/G]CTGATGGTTTTATAAATGGGAGTTC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604419
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Literature Links: |
POLQ 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 |
| POLQ - DNA polymerase theta | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_199420.3 | Intron | NP_955452.3 | ||||
| XM_011512343.2 | Intron | XP_011510645.1 | ||||
| XM_011512347.2 | Intron | XP_011510649.1 | ||||
| XM_011512348.2 | Intron | XP_011510650.1 | ||||
| XM_011512352.2 | Intron | XP_011510654.1 | ||||
| XM_011512354.2 | Intron | XP_011510656.1 | ||||
| XM_017005565.1 | Intron | XP_016861054.1 | ||||
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