Product Details

SNP ID
rs34091519
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:15660441 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTCACATGACCAAGAATATCTTTG[G/T]AACATAGGGGACCTTGAGCTTCCTG
Phenotype
MIM: 601966
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
DDI2 PubMed Links

Gene Details

Gene
DDI2
Gene Name
DNA damage inducible 1 homolog 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032341.4 729 UTR 3 NP_115717.3
Gene
RSC1A1
Gene Name
regulatory solute carrier protein, family 1, member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006511.2 729 Missense Mutation TGG,TGT W191C NP_006502.1

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