Product Details
- SNP ID
-
rs202221844
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:172102427 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTGCTGCTGCTGCTGCTGTTGCCAC[C/T]CGGGCCGGCGCCGCCGCCGCTCGGG
- Phenotype
-
MIM: 126255
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
DLX2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs554191002] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- DLX2
- Gene Name
- distal-less homeobox 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_004405.3 |
324 |
Missense Mutation |
AGT,GGT |
S38G |
NP_004396.1 |
- Gene
- DLX2-AS1
- Gene Name
- DLX2 antisense RNA 1 (head to head)
There are no transcripts associated with this gene.
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