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- SNP ID:
- rs369940083
- Gene
-
CERS3 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.15: 100496793 - 100496793 on Build GRCh38
- Polymorphism:
- T/A, Transversion substitution
- Context Sequence [VIC/FAM]:
GACTTACTTAAGAAGAATTTTTGTG[T/A]TGAATTAAATGCTGACAATTTTAGT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615276
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Literature Links: |
CERS3 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 |
| CERS3 - ceramide synthase 3 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001290341.2 | Intron | NP_001277270.1 | ||||
| NM_001290342.2 | Intron | NP_001277271.1 | ||||
| NM_001290343.1 | Intron | NP_001277272.1 | ||||
| NM_178842.4 | Intron | NP_849164.2 | ||||
| XM_011521355.2 | Intron | XP_011519657.1 | ||||
| XM_011521357.2 | Intron | XP_011519659.1 | ||||
| XM_011521358.1 | Intron | XP_011519660.1 | ||||
| XM_017022002.1 | Intron | XP_016877491.1 | ||||
| XM_017022003.1 | Intron | XP_016877492.1 | ||||
| XM_017022004.1 | Intron | XP_016877493.1 | ||||
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