Product Details

SNP ID

rs201511730

Assay Type

Functionally tested

NCBI dbSNP Submissions

11

Location

Chr.1:92513697 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACGACTCTCTTCTTCTCGGGGGCC[A/G]CTCCTTTTGAACCACTTGGTTGCTC

Phenotype

MIM: 602942

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

EVI5 PubMed Links

Gene Details

Gene

EVI5

Gene Name

ecotropic viral integration site 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308248.1	2514	Missense Mutation	CGG,TGG	R809W	NP_001295177.1
NM_005665.5	2514	Missense Mutation	CGG,TGG	R798W	NP_005656.4
XM_017002269.1	2514	Missense Mutation	CGG,TGG	R918W	XP_016857758.1
XM_017002270.1	2514	Missense Mutation	CGG,TGG	R915W	XP_016857759.1
XM_017002271.1	2514	Missense Mutation	CGG,TGG	R891W	XP_016857760.1
XM_017002272.1	2514	Missense Mutation	CGG,TGG	R885W	XP_016857761.1
XM_017002273.1	2514	Missense Mutation	CGG,TGG	R874W	XP_016857762.1
XM_017002274.1	2514	Missense Mutation	CGG,TGG	R874W	XP_016857763.1
XM_017002275.1	2514	Missense Mutation	CGG,TGG	R874W	XP_016857764.1
XM_017002276.1	2514	Missense Mutation	CGG,TGG	R847W	XP_016857765.1
XM_017002277.1	2514	Missense Mutation	CGG,TGG	R842W	XP_016857766.1
XM_017002278.1	2514	Missense Mutation	CGG,TGG	R836W	XP_016857767.1
XM_017002279.1	2514	Missense Mutation	CGG,TGG	R829W	XP_016857768.1
XM_017002280.1	2514	Missense Mutation	CGG,TGG	R814W	XP_016857769.1
XM_017002281.1	2514	Missense Mutation	CGG,TGG	R806W	XP_016857770.1
XM_017002282.1	2514	UTR 3			XP_016857771.1
XM_017002283.1	2514	UTR 3			XP_016857772.1
XM_017002284.1	2514	Missense Mutation	CGG,TGG	R765W	XP_016857773.1
XM_017002285.1	2514	UTR 3			XP_016857774.1
XM_017002286.1	2514	Missense Mutation	CGG,TGG	R710W	XP_016857775.1
XM_017002287.1	2514	Missense Mutation	CGG,TGG	R710W	XP_016857776.1
XM_017002288.1	2514	Missense Mutation	CGG,TGG	R710W	XP_016857777.1

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