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SNP ID

rs144340720

Assay Type

Functionally tested

NCBI dbSNP Submissions

15

Location

Chr.1:15626766 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTGTGATTTTACGACAGAAGGAGA[A/G]TGCAGACCCTCGACCTCCAGTGCAG

Phenotype

Polymorphism

A/G, Transition 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	449	Missense Mutation	AAT,AGT	N79S	NP_115717.3

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