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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