Product Details

SNP ID

rs1802887

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:10393273 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGAGCCCCACCTCAGGGAGGGACT[A/C]GTAGACCTCGACGGGGTCCAGGCCG

Phenotype

MIM: 605065

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

CDC37 PubMed Links

Gene Details

Gene

CDC37

Gene Name

cell division cycle 37

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007065.3		Intron			NP_008996.1
XM_011527652.2		Intron			XP_011525954.1

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