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- SNP ID:
- rs145038000
- Gene
-
PDCD5 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 32584962 - 32584962 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
GTTTTCGTTGTAGGGAAGCAGAAAT[A/G]AGAAACAGTATCTTAGCCCAAGTTC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604583
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Literature Links: |
PDCD5 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 |
| PDCD5 - programmed cell death 5 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_004708.3 | 218 | Intron | NP_004699.1 | |||
| XM_005259392.4 | 218 | Missense Mutation | ATA,ATG | I,M 39 | XP_005259449.1 | |
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