Product Details

SNP ID: rs139203737
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:72274812 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTGCAGGAGAGCCTGGCCCAGGCGC[A/G]GCTGGGCTCTCGACGCCCTGCGCGC
Phenotype: MIM: 607729
Polymorphism: A/G, 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	525	Missense Mutation	CAG,CGG	Q108R	NP_061931.1