Product Details

SNP ID

rs951300

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:149737864 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAGAAGATACTTAATCAAATTCAT[A/G]TAAGTACAGAGAAGACTGAGTAAGT

Phenotype

MIM: 616699

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

COMMD2 PubMed Links

Gene Details

Gene

COMMD2

Gene Name

COMM domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016094.3		Intron			NP_057178.2

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