Product Details
- SNP ID
-
rs61750804
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
2
- Location
-
Chr.1:77697885 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TACCTTGCCTAAGCATCACATTACC[A/G]CATTTAGTGACTGCAATCTTAGTAT
- Phenotype
-
MIM: 615146
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
USP33
PubMed Links
Gene Details
- Gene
- USP33
- Gene Name
- ubiquitin specific peptidase 33
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_015017.4 |
3023 |
Silent Mutation |
TGC,TGT |
C883C |
NP_055832.3 |
NM_201624.2 |
3023 |
Silent Mutation |
TGC,TGT |
C852C |
NP_963918.1 |
NM_201626.2 |
3023 |
Intron |
|
|
NP_963920.1 |
XM_005270648.1 |
3023 |
Silent Mutation |
TGC,TGT |
C875C |
XP_005270705.1 |
XM_005270649.1 |
3023 |
Missense Mutation |
GCG,GTG |
A849V |
XP_005270706.1 |
XM_011541055.1 |
3023 |
Silent Mutation |
TGC,TGT |
C784C |
XP_011539357.1 |
XM_011541056.2 |
3023 |
Intron |
|
|
XP_011539358.1 |
XM_017000722.1 |
3023 |
Silent Mutation |
TGC,TGT |
C844C |
XP_016856211.1 |
XM_017000723.1 |
3023 |
Missense Mutation |
GCG,GTG |
A818V |
XP_016856212.1 |
XM_017000724.1 |
3023 |
Missense Mutation |
GCG,GTG |
A810V |
XP_016856213.1 |
XM_017000725.1 |
3023 |
Silent Mutation |
TGC,TGT |
C753C |
XP_016856214.1 |
XM_017000726.1 |
3023 |
Silent Mutation |
TGC,TGT |
C745C |
XP_016856215.1 |
XM_017000727.1 |
3023 |
Silent Mutation |
TGC,TGT |
C704C |
XP_016856216.1 |
XM_017000728.1 |
3023 |
Silent Mutation |
TGC,TGT |
C704C |
XP_016856217.1 |
XM_017000729.1 |
3023 |
Missense Mutation |
GCG,GTG |
A750V |
XP_016856218.1 |
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