Product Details

SNP ID

rs10046568

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:13893466 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAATTATGTATTTAGTTCAGTGAGT[C/T]ACTACGTTAAAACAGCAAAACATAT

Phenotype

MIM: 600541

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ETV1 PubMed Links

Gene Details

Gene

ETV1

Gene Name

ETS variant 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001163147.1	4052	UTR 3			NP_001156619.1
NM_001163148.1	4052	UTR 3			NP_001156620.1
NM_001163149.1	4052	UTR 3			NP_001156621.1
NM_001163150.1	4052	UTR 3			NP_001156622.1
NM_001163151.1	4052	UTR 3			NP_001156623.1
NM_001163152.1	4052	UTR 3			NP_001156624.1
NM_004956.4	4052	UTR 3			NP_004947.2
XM_005249635.4	4052	UTR 3			XP_005249692.1
XM_005249636.4	4052	UTR 3			XP_005249693.1
XM_011515167.2	4052	UTR 3			XP_011513469.1
XM_011515168.2	4052	UTR 3			XP_011513470.1
XM_011515170.2	4052	UTR 3			XP_011513472.1

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