Product Details

SNP ID
rs144579601
Assay Type
Functionally tested
NCBI dbSNP Submissions
5
Location
Chr.1:157093025 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTCCAGTTGGAGGGCAGAGGGGGC[A/G]GGAGGGGAGGAGTGAAGGAGGCAAC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
ETV3L PubMed Links

Gene Details

Gene
ETV3L
Gene Name
ETS variant 3 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001004341.2 995 Missense Mutation CCG,CTG P237L NP_001004341.1

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