Product Details
- SNP ID
-
rs202089278
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:35619747 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTCAGTGTGCGTGTTCCGCGAGCGG[A/G]CCGCGCGGCGCGTCCTGGAGCTGCA
- Phenotype
-
MIM: 612206
- Polymorphism
- A/G, Transition 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 |
1561 |
Missense Mutation |
ACC,GCC |
T371A |
NP_055159.2 |
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