Product Details

SNP ID

rs7645816

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:138951853 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCCTCCACTTCTCACTCAGTGCT[C/T]CCCACCAGGATGGGCTTAATGCCTT

Phenotype

MIM: 605597

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FOXL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs200854858] 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

FOXL2

Gene Name

forkhead box L2

There are no transcripts associated with this gene.

Gene

FOXL2NB

Gene Name

FOXL2 neighbor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040061.2	1940	UTR 3			NP_001035150.1
XM_005247443.3	1940	UTR 3			XP_005247500.1

Gene

LINC01391

Gene Name

long intergenic non-protein coding RNA 1391

There are no transcripts associated with this gene.

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