Product Details

SNP ID
rs11202914
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:88970454 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTAGGCCCCTGCTTGTTGAGGAGGG[C/T]GTTCAGTTAGTGCTGAGACTACCTG
Phenotype
MIM: 102620 MIM: 134637
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
ACTA2 PubMed Links
Additional Information
For this assay, SNP(s) [rs113631043] 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
ACTA2
Gene Name
actin, alpha 2, smooth muscle, aorta
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001141945.2 2026 Intron NP_001135417.1
NM_001320855.1 2026 Intron NP_001307784.1
NM_001613.2 2026 Intron NP_001604.1
Gene
FAS
Gene Name
Fas cell surface death receptor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000043.5 2026 Intron NP_000034.1
NM_001320619.1 2026 Intron NP_001307548.1
NM_152871.3 2026 Intron NP_690610.1
NM_152872.3 2026 Intron NP_690611.1
XM_006717819.3 2026 UTR 5 XP_006717882.1
XM_011539764.2 2026 Intron XP_011538066.1
XM_011539765.2 2026 Intron XP_011538067.1
XM_011539766.2 2026 Intron XP_011538068.1
XM_011539767.2 2026 Intron XP_011538069.1

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