Product Details
- SNP ID
-
rs117785251
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:75591675 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAAAAGATCATGCAGTTCCTAAGCA[G/T]CCTGGAGCAGGATCAGACGGGGAAC
- Phenotype
-
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
MYO15B
PubMed Links
Gene Details
- Gene
- MYO15B
- Gene Name
- myosin XVB
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001309242.1 |
2369 |
Missense Mutation |
AGC,ATC |
S837I |
NP_001296171.1 |
XM_017025120.1 |
2369 |
Missense Mutation |
AGC,ATC |
S619I |
XP_016880609.1 |
XM_017025121.1 |
2369 |
Missense Mutation |
AGC,ATC |
S614I |
XP_016880610.1 |
XM_017025122.1 |
2369 |
Missense Mutation |
AGC,ATC |
S619I |
XP_016880611.1 |
XM_017025123.1 |
2369 |
Missense Mutation |
AGC,ATC |
S619I |
XP_016880612.1 |
XM_017025124.1 |
2369 |
Missense Mutation |
AGC,ATC |
S619I |
XP_016880613.1 |
XM_017025125.1 |
2369 |
Missense Mutation |
AGC,ATC |
S619I |
XP_016880614.1 |
XM_017025126.1 |
2369 |
Missense Mutation |
AGC,ATC |
S619I |
XP_016880615.1 |
XM_017025127.1 |
2369 |
Missense Mutation |
AGC,ATC |
S390I |
XP_016880616.1 |
XM_017025128.1 |
2369 |
Missense Mutation |
AGC,ATC |
S381I |
XP_016880617.1 |
XM_017025129.1 |
2369 |
Missense Mutation |
AGC,ATC |
S98I |
XP_016880618.1 |
XM_017025130.1 |
2369 |
Missense Mutation |
AGC,ATC |
S90I |
XP_016880619.1 |
XM_017025131.1 |
2369 |
Missense Mutation |
AGC,ATC |
S55I |
XP_016880620.1 |
XM_017025132.1 |
2369 |
UTR 5 |
|
|
XP_016880621.1 |
XM_017025133.1 |
2369 |
UTR 5 |
|
|
XP_016880622.1 |
XM_017025134.1 |
2369 |
UTR 5 |
|
|
XP_016880623.1 |
XM_017025135.1 |
2369 |
Intron |
|
|
XP_016880624.1 |
XM_017025136.1 |
2369 |
Intron |
|
|
XP_016880625.1 |
XM_017025137.1 |
2369 |
Intron |
|
|
XP_016880626.1 |
XM_017025138.1 |
2369 |
Intron |
|
|
XP_016880627.1 |
XM_017025139.1 |
2369 |
Intron |
|
|
XP_016880628.1 |
XM_017025140.1 |
2369 |
Intron |
|
|
XP_016880629.1 |
XM_017025141.1 |
2369 |
Missense Mutation |
AGC,ATC |
S619I |
XP_016880630.1 |
XM_017025142.1 |
2369 |
Missense Mutation |
AGC,ATC |
S619I |
XP_016880631.1 |
XM_017025143.1 |
2369 |
Intron |
|
|
XP_016880632.1 |
XM_017025144.1 |
2369 |
UTR 5 |
|
|
XP_016880633.1 |
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