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- SNP ID:
- rs765938149
- Gene
-
PPT1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 40097221 - 40097221 on Build GRCh38
- Polymorphism:
- G/A, Transition substitution
- Context Sequence [VIC/FAM]:
GGAGAGCCACAGCCAAGAGCCACAG[G/A]CAGCCGGGCGACGCCATCTTCGCTG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 600722
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Literature Links: |
PPT1 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 |
| PPT1 - palmitoyl-protein thioesterase 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_000310.3 | 250 | Silent Mutation | TGC,TGT | C,C 6 | NP_000301.1 | |
| NM_001142604.1 | 250 | Silent Mutation | TGC,TGT | C,C 6 | NP_001136076.1 | |
| XM_005271008.1 | 250 | Silent Mutation | TGC,TGT | C,C 6 | XP_005271065.1 | |
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