Product Details

SNP ID

rs4713964

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.6:36361641 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTATGAAGGAAAAAGCCTTTCTAAG[A/C]AAGAATCCACCTAACAGAGAAGAGG

Phenotype

MIM: 605255

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

ETV7 PubMed Links

Additional Information

For this assay, SNP(s) [rs73729955] 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

ETV7

Gene Name

ETS variant 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001207035.1		Intron			NP_001193964.1
NM_001207036.1		Intron			NP_001193965.1
NM_001207037.1		Intron			NP_001193966.1
NM_001207038.1		Intron			NP_001193967.1
NM_001207039.1		Intron			NP_001193968.1
NM_001207040.1		Intron			NP_001193969.1
NM_001207041.1		Intron			NP_001193970.1
NM_016135.3		Intron			NP_057219.1
XM_011514659.1		Intron			XP_011512961.1

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