Product Details

SNP ID

rs200274419

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:82914768 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACAGAAGACGAAAATTTCTTCTAGC[C/G]TCAGTACTTGCTCTCCAGAATTCAA

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

DDIAS PubMed Links

Additional Information

For this assay, SNP(s) [rs61902276] 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

DDIAS

Gene Name

DNA damage induced apoptosis suppressor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145018.3	136	Silent Mutation	GCC,GCG	A10A	NP_659455.3
XM_011544835.1	136	Silent Mutation	GCC,GCG	A10A	XP_011543137.1
XM_011544836.2	136	Silent Mutation	GCC,GCG	A10A	XP_011543138.1
XM_011544837.1	136	Intron			XP_011543139.1
XM_011544838.2	136	UTR 5			XP_011543140.1
XM_017017352.1	136	UTR 5			XP_016872841.1
XM_017017353.1	136	UTR 5			XP_016872842.1

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