Product Details
- SNP ID
-
rs112923895
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.14:74241207 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ATTCTGAAGATGTTTCCTCCAGCGA[C/T]CGAAAAATGTCCAAATCTGCTTTAA
- Phenotype
-
MIM: 142993
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
VSX2
PubMed Links
Gene Details
- Gene
- VSX2
- Gene Name
- visual system homeobox 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_182894.2 |
486 |
Silent Mutation |
GAC,GAT |
D132D |
NP_878314.1 |
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