Product Details
- SNP ID
-
rs115264746
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:196472257 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GATGCTCCAAATCTATCAGTTTTTG[A/G]GTAAAGTTTATTTCTGTTTCCTCTT
- Phenotype
-
MIM: 612688
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
RNF168
PubMed Links
Gene Details
- Gene
- RNF168
- Gene Name
- ring finger protein 168
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_152617.3 |
1873 |
Silent Mutation |
ACC,ACT |
T426T |
NP_689830.2 |
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