Product Details

SNP ID

rs3773305

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.3:12837054 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ATGAGTCCACTCAAATTCAAAGCAA[C/T]TGTATTTTTAAATGTTTCTACGTTT

Phenotype

MIM: 610403

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CAND2 PubMed Links

Additional Information

For this assay, SNP(s) [rs80067234] 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

CAND2

Gene Name

cullin associated and neddylation dissociated 2 (putative)

There are no transcripts associated with this gene.

Gene

RPL32

Gene Name

ribosomal protein L32

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000994.3		Intron			NP_000985.1
NM_001007073.1		Intron			NP_001007074.1
NM_001007074.1		Intron			NP_001007075.1

Gene

SNORA7A

Gene Name

small nucleolar RNA, H/ACA box 7A

There are no transcripts associated with this gene.

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