Product Details

SNP ID

rs148841919

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:67930469 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACGTGAGGCCTTCAGTCAGAGCCTC[G/T]TTTGAGGATGCCAGGCAAACTGGCG

Phenotype

MIM: 118888 MIM: 606967 MIM: 177015 MIM: 176847

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CTRL PubMed Links

Additional Information

For this assay, SNP(s) [rs11552953] 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

CTRL

Gene Name

chymotrypsin like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001907.2	461	Silent Mutation			NP_001898.1

Gene

LCAT

Gene Name

lecithin-cholesterol acyltransferase

There are no transcripts associated with this gene.

Gene

PSKH1

Gene Name

protein serine kinase H1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006742.2	461	Intron			NP_006733.1

Gene

PSMB10

Gene Name

proteasome subunit beta 10

There are no transcripts associated with this gene.

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