Product Details

SNP ID
rs79984518
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:2018385 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTTCCTCCTCCCTAACCTGATGG[A/C]GGTTGGTGCTTTGGAAAAAGCAAAG
Phenotype
MIM: 600014
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
SMARCA2 PubMed Links
Additional Information
For this assay, SNP(s) [rs144514367] 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
SMARCA2
Gene Name
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001289396.1 Intron NP_001276325.1
NM_001289397.1 Intron NP_001276326.1
NM_001289398.1 Intron NP_001276327.1
NM_001289399.1 Intron NP_001276328.1
NM_001289400.1 Intron NP_001276329.1
NM_003070.4 Intron NP_003061.3
NM_139045.3 Intron NP_620614.2

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