Product Details

SNP ID

rs10204260

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:196651663 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCGATAGTCTAGTATGGGTTCTCTT[G/T]TATGTAACAAGCTACTTTTCCCTTG

Phenotype

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CCDC150 PubMed Links

Additional Information

For this assay, SNP(s) [rs75077800] 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

CCDC150

Gene Name

coiled-coil domain containing 150

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080539.1		Intron			NP_001074008.1
XM_006712438.3		Intron			XP_006712501.1
XM_006712439.3		Intron			XP_006712502.1
XM_011510985.2		Intron			XP_011509287.1
XM_011510987.2		Intron			XP_011509289.1
XM_011510988.2		Intron			XP_011509290.1
XM_017003861.1		Intron			XP_016859350.1
XM_017003862.1		Intron			XP_016859351.1
XM_017003863.1		Intron			XP_016859352.1
XM_017003864.1		Intron			XP_016859353.1
XM_017003865.1		Intron			XP_016859354.1
XM_017003866.1		Intron			XP_016859355.1

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