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- SNP ID:
- rs200336029
- Gene
-
DCLK2LRBA - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.4: 150265753 - 150265753 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
GCGGGTTTGGTATTCATGATGCCAC[C/T]GGTTAAAGTCGTTGTAAAATAGCAC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613166
MIM: 606453
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Literature Links: |
DCLK2 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 |
| DCLK2 - doublecortin like kinase 2 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| LRBA - LPS responsive beige-like anchor protein | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001199282.2 | 9015 | Missense Mutation | CAG,CGG | Q,R 2842 | NP_001186211.2 | |
| NM_006726.4 | 9015 | Missense Mutation | CAG,CGG | Q,R 2854 | NP_006717.2 | |
| XM_005263372.3 | 9015 | Missense Mutation | CAG,CGG | Q,R 2859 | XP_005263429.1 | |
| XM_005263373.2 | 9015 | Missense Mutation | CAG,CGG | Q,R 2859 | XP_005263430.1 | |
| XM_005263374.3 | 9015 | Missense Mutation | CAG,CGG | Q,R 2848 | XP_005263431.1 | |
| XM_005263375.3 | 9015 | Missense Mutation | CAG,CGG | Q,R 2843 | XP_005263432.1 | |
| XM_011532434.2 | 9015 | Missense Mutation | CAG,CGG | Q,R 2854 | XP_011530736.1 | |
| XM_017008872.1 | 9015 | Missense Mutation | CAG,CGG | Q,R 2848 | XP_016864361.1 | |
| XM_017008873.1 | 9015 | Missense Mutation | CAG,CGG | Q,R 749 | XP_016864362.1 | |
| XM_017008874.1 | 9015 | Missense Mutation | CAG,CGG | Q,R 747 | XP_016864363.1 | |
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