Product Details
- SNP ID
-
rs2290455
- Assay Type
- Validated
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:75591187 on Build GRCh38
- Set Membership
-
HapMap
Validated
- Context Sequence [VIC/FAM]
- TCTCCCTCAGACACATCTTTGCCAT[C/T]GTGGCATCAGCCTATGACCTGGCTC
- Phenotype
-
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
MYO15B
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs80252608] are located under a probe and SNP(s) [rs147655466] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- MYO15B
- Gene Name
- myosin XVB
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001309242.1 |
2235 |
Silent Mutation |
ATC,ATT |
I792I |
NP_001296171.1 |
| XM_017025120.1 |
2235 |
Silent Mutation |
ATC,ATT |
I574I |
XP_016880609.1 |
| XM_017025121.1 |
2235 |
Silent Mutation |
ATC,ATT |
I574I |
XP_016880610.1 |
| XM_017025122.1 |
2235 |
Silent Mutation |
ATC,ATT |
I574I |
XP_016880611.1 |
| XM_017025123.1 |
2235 |
Silent Mutation |
ATC,ATT |
I574I |
XP_016880612.1 |
| XM_017025124.1 |
2235 |
Silent Mutation |
ATC,ATT |
I574I |
XP_016880613.1 |
| XM_017025125.1 |
2235 |
Silent Mutation |
ATC,ATT |
I574I |
XP_016880614.1 |
| XM_017025126.1 |
2235 |
Silent Mutation |
ATC,ATT |
I574I |
XP_016880615.1 |
| XM_017025127.1 |
2235 |
Silent Mutation |
ATC,ATT |
I345I |
XP_016880616.1 |
| XM_017025128.1 |
2235 |
Silent Mutation |
ATC,ATT |
I336I |
XP_016880617.1 |
| XM_017025129.1 |
2235 |
Silent Mutation |
ATC,ATT |
I53I |
XP_016880618.1 |
| XM_017025130.1 |
2235 |
Silent Mutation |
ATC,ATT |
I50I |
XP_016880619.1 |
| XM_017025131.1 |
2235 |
Silent Mutation |
ATC,ATT |
I15I |
XP_016880620.1 |
| XM_017025132.1 |
2235 |
UTR 5 |
|
|
XP_016880621.1 |
| XM_017025133.1 |
2235 |
Intron |
|
|
XP_016880622.1 |
| XM_017025134.1 |
2235 |
UTR 5 |
|
|
XP_016880623.1 |
| XM_017025135.1 |
2235 |
Intron |
|
|
XP_016880624.1 |
| XM_017025136.1 |
2235 |
Intron |
|
|
XP_016880625.1 |
| XM_017025137.1 |
2235 |
Intron |
|
|
XP_016880626.1 |
| XM_017025138.1 |
2235 |
Intron |
|
|
XP_016880627.1 |
| XM_017025139.1 |
2235 |
Intron |
|
|
XP_016880628.1 |
| XM_017025140.1 |
2235 |
Intron |
|
|
XP_016880629.1 |
| XM_017025141.1 |
2235 |
Silent Mutation |
ATC,ATT |
I574I |
XP_016880630.1 |
| XM_017025142.1 |
2235 |
Silent Mutation |
ATC,ATT |
I574I |
XP_016880631.1 |
| XM_017025143.1 |
2235 |
Intron |
|
|
XP_016880632.1 |
| XM_017025144.1 |
2235 |
UTR 5 |
|
|
XP_016880633.1 |
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