Product Details

SNP ID

rs150594486

Assay Type

Functionally Tested

NCBI dbSNP Submissions

6

Location

Chr.1:42534954 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGAAGATAGAAGAGAAACCAGTAC[A/T]AAAGATCAAGAGACAAAGTACAAGA

Phenotype

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

CCDC30 PubMed Links

Additional Information

For this assay, SNP(s) [rs200019270] 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

CCDC30

Gene Name

coiled-coil domain containing 30

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080850.2	998	UTR 5			NP_001074319.1
XM_011542067.2	998	UTR 5			XP_011540369.1
XM_011542068.2	998	UTR 5			XP_011540370.1
XM_011542069.2	998	UTR 5			XP_011540371.1
XM_011542070.2	998	Intron			XP_011540372.1
XM_011542071.2	998	UTR 5			XP_011540373.1
XM_017002225.1	998	UTR 5			XP_016857714.1
XM_017002226.1	998	UTR 5			XP_016857715.1

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