Product Details
- SNP ID
-
rs202002402
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:99613035 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTTTTCCATTCTTTCTTGCCCAGGG[A/G]AGGAGCGCTACATCTGCTGGTACTG
- Phenotype
-
MIM: 616741
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
PRDM13
PubMed Links
Gene Details
- Gene
- PRDM13
- Gene Name
- PR domain 13
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_021620.3 |
661 |
Missense Mutation |
AAG,GAG |
K134E |
NP_067633.2 |
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