Product Details

SNP ID
rs28557435
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:13892976 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGTGGTAATTGGTTACAGCATCTA[C/T]GGGAAACTAGACCTCCAAGATCCGC
Phenotype
MIM: 600541
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
ETV1 PubMed Links
Additional Information
For this assay, SNP(s) [rs76169013] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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 4542 UTR 3 NP_001156619.1
NM_001163148.1 4542 UTR 3 NP_001156620.1
NM_001163149.1 4542 UTR 3 NP_001156621.1
NM_001163150.1 4542 UTR 3 NP_001156622.1
NM_001163151.1 4542 UTR 3 NP_001156623.1
NM_001163152.1 4542 UTR 3 NP_001156624.1
NM_004956.4 4542 UTR 3 NP_004947.2
XM_005249635.4 4542 Intron XP_005249692.1
XM_005249636.4 4542 Intron XP_005249693.1
XM_011515167.2 4542 Intron XP_011513469.1
XM_011515168.2 4542 Intron XP_011513470.1
XM_011515170.2 4542 Intron XP_011513472.1

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