Product Details

SNP ID: rs145979821
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:72274351 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CGACCCGGGAGGAGGGGTTTGACCG[C/T]TCCACGAGCCTGGAGAGCTCGGACT
Phenotype: MIM: 607729
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: DDIT4 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019058.2	337	Silent Mutation	CGC,CGT	R45R	NP_061931.1