Product Details

SNP ID

rs2782828

Assay Type

Validated

NCBI dbSNP Submissions

40

Location

Chr.1:207323654 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

AACAACTTAAATCAATAGAAGCTAC[G/T]GTAAATACAGAAATTGGCACAAATA

Phenotype

MIM: 125240

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CD55 PubMed Links

Additional Information

For this assay, SNP(s) [rs28371598] 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

CD55

Gene Name

CD55 molecule (Cromer blood group)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000574.4		Intron			NP_000565.1
NM_001114752.2		Intron			NP_001108224.1
NM_001300902.1		Intron			NP_001287831.1
NM_001300903.1		Intron			NP_001287832.1
NM_001300904.1		Intron			NP_001287833.1
XM_017000467.1		Intron			XP_016855956.1

View Full Product Details