Product Details

SNP ID

rs9809596

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.3:12799014 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

CCTGGCTTTATGGGCAGGAGGTGCC[C/G]CATTACCACGGAGGCTCCAGCAGTC

Phenotype

MIM: 610403

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CAND2 PubMed Links

Gene Details

Gene

CAND2

Gene Name

cullin associated and neddylation dissociated 2 (putative)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001162499.1		Intron			NP_001155971.1
NM_012298.2		Intron			NP_036430.1
XM_011533503.2		Intron			XP_011531805.1
XM_011533504.2		Intron			XP_011531806.1

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