Product Details

SNP ID

rs200275281

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:39504079 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCTCTGTCCCCCATAGTGGTGTGC[C/G]GAGCAGGCTGCAGCCCTGAGCATGG

Phenotype

MIM: 602768

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

DLL3 PubMed Links

Gene Details

Gene

DLL3

Gene Name

delta like canonical Notch ligand 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016941.3	719	Missense Mutation	CGA,GGA	R221G	NP_058637.1
NM_203486.2	719	Missense Mutation	CGA,GGA	R221G	NP_982353.1

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