Product Details
- SNP ID
-
rs202207556
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
3
- Location
-
Chr.1:42179768 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GATGTCATCTGGAGGCAGGGAACGC[C/T]GCATCTGGAAGGCTTGGGAAGGCAT
- Phenotype
-
MIM: 616035
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FOXJ3
PubMed Links
Gene Details
- Gene
- FOXJ3
- Gene Name
- forkhead box J3
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001198850.1 |
2027 |
Missense Mutation |
CAG,CGG |
Q604R |
NP_001185779.1 |
| NM_001198851.1 |
2027 |
Missense Mutation |
CAG,CGG |
Q604R |
NP_001185780.1 |
| NM_001198852.1 |
2027 |
Missense Mutation |
CAG,CGG |
Q570R |
NP_001185781.1 |
| NM_014947.4 |
2027 |
Missense Mutation |
CAG,CGG |
Q604R |
NP_055762.3 |
| XM_005270632.4 |
2027 |
Missense Mutation |
CAG,CGG |
Q612R |
XP_005270689.1 |
| XM_006710458.3 |
2027 |
Missense Mutation |
CAG,CGG |
Q589R |
XP_006710521.1 |
| XM_006710459.3 |
2027 |
Missense Mutation |
CAG,CGG |
Q578R |
XP_006710522.1 |
| XM_011541026.2 |
2027 |
Missense Mutation |
CAG,CGG |
Q604R |
XP_011539328.1 |
| XM_017000693.1 |
2027 |
Missense Mutation |
CAG,CGG |
Q555R |
XP_016856182.1 |
| XM_017000694.1 |
2027 |
Missense Mutation |
CAG,CGG |
Q502R |
XP_016856183.1 |
| XM_017000695.1 |
2027 |
Missense Mutation |
CAG,CGG |
Q415R |
XP_016856184.1 |
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