Product Details
- SNP ID
-
rs201614496
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:113799321 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGCTACATAGGTCATAGGGAGAATT[G/T]GGTCGAATAGTTGGAGGCTCTTTCA
- Phenotype
-
MIM: 610748
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
LOC390251
PubMed Links
Gene Details
- Gene
- LOC390251
- Gene Name
- SH3 domain containing GRB2 like 1 pseudogene
There are no transcripts associated with this gene.
- Gene
- USP28
- Gene Name
- ubiquitin specific peptidase 28
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001301029.1 |
3407 |
Silent Mutation |
CCA,CCC |
P894P |
NP_001287958.1 |
NM_020886.3 |
3407 |
Silent Mutation |
CCA,CCC |
P1051P |
NP_065937.1 |
XM_005271630.2 |
3407 |
Silent Mutation |
CCA,CCC |
P1114P |
XP_005271687.1 |
XM_005271631.2 |
3407 |
Silent Mutation |
CCA,CCC |
P1113P |
XP_005271688.1 |
XM_005271632.2 |
3407 |
Silent Mutation |
CCA,CCC |
P1111P |
XP_005271689.1 |
XM_005271633.4 |
3407 |
Silent Mutation |
CCA,CCC |
P1092P |
XP_005271690.1 |
XM_005271636.2 |
3407 |
Silent Mutation |
CCA,CCC |
P1054P |
XP_005271693.1 |
XM_005271637.2 |
3407 |
Silent Mutation |
CCA,CCC |
P1052P |
XP_005271694.1 |
XM_005271638.2 |
3407 |
Silent Mutation |
CCA,CCC |
P1020P |
XP_005271695.1 |
XM_005271639.2 |
3407 |
Silent Mutation |
CCA,CCC |
P1019P |
XP_005271696.1 |
XM_011542936.2 |
3407 |
Silent Mutation |
CCA,CCC |
P1088P |
XP_011541238.1 |
XM_011542938.1 |
3407 |
Silent Mutation |
CCA,CCC |
P989P |
XP_011541240.1 |
XM_011542941.1 |
3407 |
Silent Mutation |
CCA,CCC |
P761P |
XP_011541243.1 |
XM_011542942.1 |
3407 |
Silent Mutation |
CCA,CCC |
P670P |
XP_011541244.1 |
XM_017018056.1 |
3407 |
Silent Mutation |
CCA,CCC |
P1087P |
XP_016873545.1 |
XM_017018057.1 |
3407 |
Silent Mutation |
CCA,CCC |
P1048P |
XP_016873546.1 |
XM_017018058.1 |
3407 |
Silent Mutation |
CCA,CCC |
P1025P |
XP_016873547.1 |
XM_017018059.1 |
3407 |
Silent Mutation |
CCA,CCC |
P993P |
XP_016873548.1 |
XM_017018060.1 |
3407 |
Silent Mutation |
CCA,CCC |
P988P |
XP_016873549.1 |
XM_017018061.1 |
3407 |
Silent Mutation |
CCA,CCC |
P927P |
XP_016873550.1 |
XM_017018062.1 |
3407 |
Silent Mutation |
CCA,CCC |
P926P |
XP_016873551.1 |
XM_017018063.1 |
3407 |
Silent Mutation |
CCA,CCC |
P826P |
XP_016873552.1 |
XM_017018064.1 |
3407 |
Silent Mutation |
CCA,CCC |
P764P |
XP_016873553.1 |
XM_017018065.1 |
3407 |
Silent Mutation |
CCA,CCC |
P699P |
XP_016873554.1 |
XM_017018066.1 |
3407 |
Silent Mutation |
CCA,CCC |
P699P |
XP_016873555.1 |
XM_017018067.1 |
3407 |
Silent Mutation |
CCA,CCC |
P699P |
XP_016873556.1 |
XM_017018068.1 |
3407 |
Silent Mutation |
CCA,CCC |
P667P |
XP_016873557.1 |
XM_017018069.1 |
3407 |
Intron |
|
|
XP_016873558.1 |
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