Product Details

SNP ID

rs35826044

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:77697921 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGCAATCTTAGTATTGTCAATAGG[A/C]CCTGGAGGATCTAAAGGAAAAAATA

Phenotype

MIM: 615146

Polymorphism

A/C, Transversion 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	2987	Silent Mutation	GGG,GGT	G871G	NP_055832.3
NM_201624.2	2987	Silent Mutation	GGG,GGT	G840G	NP_963918.1
NM_201626.2	2987	Intron			NP_963920.1
XM_005270648.1	2987	Silent Mutation	GGG,GGT	G863G	XP_005270705.1
XM_005270649.1	2987	Missense Mutation	GGC,GTC	G837V	XP_005270706.1
XM_011541055.1	2987	Silent Mutation	GGG,GGT	G772G	XP_011539357.1
XM_011541056.2	2987	Intron			XP_011539358.1
XM_017000722.1	2987	Silent Mutation	GGG,GGT	G832G	XP_016856211.1
XM_017000723.1	2987	Missense Mutation	GGC,GTC	G806V	XP_016856212.1
XM_017000724.1	2987	Missense Mutation	GGC,GTC	G798V	XP_016856213.1
XM_017000725.1	2987	Silent Mutation	GGG,GGT	G741G	XP_016856214.1
XM_017000726.1	2987	Silent Mutation	GGG,GGT	G733G	XP_016856215.1
XM_017000727.1	2987	Silent Mutation	GGG,GGT	G692G	XP_016856216.1
XM_017000728.1	2987	Silent Mutation	GGG,GGT	G692G	XP_016856217.1
XM_017000729.1	2987	Missense Mutation	GGC,GTC	G738V	XP_016856218.1

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