Unique variants in gene E2F3

Information The variants shown are described using the NM_001949.3 transcript reference sequence.

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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
./. 1 - c.431A>G - r.(?) p.(Gln144Arg) g.20480114A>G - NM_001949.4(E2F3):c.431A>G p.(Gln144Arg) - E2F3_000001 variant could not be associated with disease phenotype PubMed: Vogelaar 2017, Journal: Vogelaar 2017 - - Germline - - - - - Marjolijn JL Ligtenberg
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