Product Details
- SNP ID
-
rs111623657
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:35619112 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCCCGGATGGTGGCCCTGGAGCGCG[C/G]GGGTTGCGGGCGCAGCTCCAACCGA
- Phenotype
-
MIM: 612206
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
FJX1
PubMed Links
Gene Details
- Gene
- FJX1
- Gene Name
- four jointed box 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_014344.3 |
926 |
Missense Mutation |
GCG,GGG |
A159G |
NP_055159.2 |
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