Product Details

SNP ID

rs3194211

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:72274331 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGCTCAGCCTGGGGGTCGGCGACC[C/G]GGGAGGAGGGGTTTGACCGCTCCAC

Phenotype

MIM: 607729

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

DDIT4 PubMed Links

Gene Details

Gene

DDIT4

Gene Name

DNA damage inducible transcript 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019058.2	317	Missense Mutation	CGG,GGG	R39G	NP_061931.1

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