Product Details
- SNP ID
-
rs145610358
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:65119801 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTCTTTTCTTTGTTTCTTTTCTAAT[A/T]CTCTTTTCCTCTCTTCCTCTTGTTC
- Phenotype
-
MIM: 608138
- Polymorphism
- A/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
PDCD7
PubMed Links
Gene Details
- Gene
- PDCD7
- Gene Name
- programmed cell death 7
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_005707.1 |
1218 |
Missense Mutation |
GAA,GTA |
E388V |
NP_005698.1 |
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