Product Details
- SNP ID
-
rs139288575
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
1
- Location
-
Chr.1:51236792 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCCTCAAATCCCCCACCTCGGATGA[A/C]ATCTCCCTGCTTCACGAGTCTCAGT
- Phenotype
-
MIM: 612598
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
RNF11
PubMed Links
Gene Details
- Gene
- RNF11
- Gene Name
- ring finger protein 11
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_014372.4 |
520 |
Missense Mutation |
GAA,GAC |
E12D |
NP_055187.1 |
View Full Product Details