Product Details

SNP ID
rs11139995
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:83244239 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTGAGTCTCATGCAGCTCTCTCTGG[C/T]GTGGGAAGGCACCCTTTTCTGGCCA
Phenotype
MIM: 607619
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FRMD3 PubMed Links
Additional Information
For this assay, SNP(s) [rs75099214] are located under a probe 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
FRMD3
Gene Name
FERM domain containing 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001244959.1 Intron NP_001231888.1
NM_001244960.1 Intron NP_001231889.1
NM_001244961.1 Intron NP_001231890.1
NM_001244962.1 Intron NP_001231891.1
NM_174938.5 Intron NP_777598.3
XM_017014588.1 Intron XP_016870077.1
XM_017014589.1 Intron XP_016870078.1
XM_017014590.1 Intron XP_016870079.1
XM_017014591.1 Intron XP_016870080.1
Gene
LOC102723989
Gene Name
uncharacterized LOC102723989
There are no transcripts associated with this gene.

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