Product Details

SNP ID

rs138799860

Assay Type

Functionally tested

NCBI dbSNP Submissions

5

Location

Chr.1:92513689 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGTTGAATACGACTCTCTTCTTCT[C/T]GGGGGCCGCTCCTTTTGAACCACTT

Phenotype

MIM: 602942

Polymorphism

C/T, 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	2522	Silent Mutation	CCA,CCG	P811P	NP_001295177.1
NM_005665.5	2522	Silent Mutation	CCA,CCG	P800P	NP_005656.4
XM_017002269.1	2522	Silent Mutation	CCA,CCG	P920P	XP_016857758.1
XM_017002270.1	2522	Silent Mutation	CCA,CCG	P917P	XP_016857759.1
XM_017002271.1	2522	Silent Mutation	CCA,CCG	P893P	XP_016857760.1
XM_017002272.1	2522	Silent Mutation	CCA,CCG	P887P	XP_016857761.1
XM_017002273.1	2522	Silent Mutation	CCA,CCG	P876P	XP_016857762.1
XM_017002274.1	2522	Silent Mutation	CCA,CCG	P876P	XP_016857763.1
XM_017002275.1	2522	Silent Mutation	CCA,CCG	P876P	XP_016857764.1
XM_017002276.1	2522	Silent Mutation	CCA,CCG	P849P	XP_016857765.1
XM_017002277.1	2522	Silent Mutation	CCA,CCG	P844P	XP_016857766.1
XM_017002278.1	2522	Silent Mutation	CCA,CCG	P838P	XP_016857767.1
XM_017002279.1	2522	Silent Mutation	CCA,CCG	P831P	XP_016857768.1
XM_017002280.1	2522	Silent Mutation	CCA,CCG	P816P	XP_016857769.1
XM_017002281.1	2522	Silent Mutation	CCA,CCG	P808P	XP_016857770.1
XM_017002282.1	2522	UTR 3			XP_016857771.1
XM_017002283.1	2522	UTR 3			XP_016857772.1
XM_017002284.1	2522	Silent Mutation	CCA,CCG	P767P	XP_016857773.1
XM_017002285.1	2522	UTR 3			XP_016857774.1
XM_017002286.1	2522	Silent Mutation	CCA,CCG	P712P	XP_016857775.1
XM_017002287.1	2522	Silent Mutation	CCA,CCG	P712P	XP_016857776.1
XM_017002288.1	2522	Silent Mutation	CCA,CCG	P712P	XP_016857777.1

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