Product Details
- SNP ID
-
rs377732811
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.22:29272395 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCTTTTGCAGCTACAGTGCTTACAC[C/T]GCCCAGCCCACTCAAGGATATGCAC
- Phenotype
-
MIM: 133450
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
EWSR1
PubMed Links
Gene Details
- Gene
- EWSR1
- Gene Name
- EWS RNA binding protein 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001163285.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
NP_001156757.1 |
| NM_001163286.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
NP_001156758.1 |
| NM_001163287.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
NP_001156759.1 |
| NM_005243.3 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
NP_005234.1 |
| NM_013986.3 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
NP_053733.2 |
| XM_005261389.3 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_005261446.1 |
| XM_005261390.4 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_005261447.1 |
| XM_011529995.2 |
149 |
Intron |
|
|
XP_011528297.1 |
| XM_011529996.2 |
149 |
Intron |
|
|
XP_011528298.1 |
| XM_011529997.1 |
149 |
Intron |
|
|
XP_011528299.1 |
| XM_011529998.1 |
149 |
Intron |
|
|
XP_011528300.1 |
| XM_011529999.2 |
149 |
Intron |
|
|
XP_011528301.1 |
| XM_011530000.1 |
149 |
Intron |
|
|
XP_011528302.1 |
| XM_011530001.2 |
149 |
Intron |
|
|
XP_011528303.1 |
| XM_011530002.2 |
149 |
Intron |
|
|
XP_011528304.1 |
| XM_017028644.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_016884133.1 |
| XM_017028645.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_016884134.1 |
| XM_017028646.1 |
149 |
Intron |
|
|
XP_016884135.1 |
| XM_017028647.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_016884136.1 |
| XM_017028648.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_016884137.1 |
| XM_017028649.1 |
149 |
Intron |
|
|
XP_016884138.1 |
| XM_017028650.1 |
149 |
Intron |
|
|
XP_016884139.1 |
| XM_017028651.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_016884140.1 |
| XM_017028652.1 |
149 |
Intron |
|
|
XP_016884141.1 |
| XM_017028653.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_016884142.1 |
| XM_017028654.1 |
149 |
Intron |
|
|
XP_016884143.1 |
| XM_017028655.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_016884144.1 |
| XM_017028656.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_016884145.1 |
| XM_017028657.1 |
149 |
Intron |
|
|
XP_016884146.1 |
| XM_017028658.1 |
149 |
Intron |
|
|
XP_016884147.1 |
| XM_017028659.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_016884148.1 |
| XM_017028660.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_016884149.1 |
| XM_017028661.1 |
149 |
Intron |
|
|
XP_016884150.1 |
| XM_017028662.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_016884151.1 |
| XM_017028663.1 |
149 |
Silent Mutation |
ACC,ACT |
T22T |
XP_016884152.1 |
| XM_017028664.1 |
149 |
Intron |
|
|
XP_016884153.1 |
| XM_017028665.1 |
149 |
Intron |
|
|
XP_016884154.1 |
| XM_017028666.1 |
149 |
Intron |
|
|
XP_016884155.1 |
- Gene
- RHBDD3
- Gene Name
- rhomboid domain containing 3
There are no transcripts associated with this gene.
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