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- SNP ID:
- rs2532234
- Gene
-
KANSL1KANSL1-AS1 - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.17: 46194900 - 46194900 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
AACATCTGCACCTAGGTTTCTGCGA[A/G]TTTCCATTTGTACTCCTAAAATCAC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612452
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Literature Links: |
KANSL1 PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
| Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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| 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)
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| EUR - Not Available | |||||
| AMR - Not Available |
| KANSL1 - KAT8 regulatory NSL complex subunit 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001193465.1 | Intron | NP_001180394.1 | ||||
| NM_001193466.1 | Intron | NP_001180395.1 | ||||
| NM_015443.3 | Intron | NP_056258.1 | ||||
| XM_006721823.1 | Intron | XP_006721886.1 | ||||
| XM_006721824.3 | Intron | XP_006721887.1 | ||||
| XM_011524628.2 | Intron | XP_011522930.1 | ||||
| XM_011524629.2 | Intron | XP_011522931.1 | ||||
| XM_011524630.2 | Intron | XP_011522932.1 | ||||
| XM_011524631.2 | Intron | XP_011522933.1 | ||||
| XM_011524632.2 | Intron | XP_011522934.1 | ||||
| XM_017024488.1 | Intron | XP_016879977.1 | ||||
| XM_017024489.1 | Intron | XP_016879978.1 | ||||
| KANSL1-AS1 - KANSL1 antisense RNA 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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HapMap