Product Details
- SNP ID
-
rs112029171
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:155458781 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CGAGAGCCCCGGCAGAACCCGCCAT[G/T]TGCGCCCGGCGCGGGCGGGCCGCTC
- Phenotype
-
MIM: 131310
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
EN2
PubMed Links
Gene Details
- Gene
- EN2
- Gene Name
- engrailed homeobox 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001427.3 |
653 |
Missense Mutation |
TGT,TTT |
C135F |
NP_001418.2 |
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