All variants in the SMARCA2 gene

Information The variants shown are described using the NM_003070.3 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

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     
+/? 18 c.2556A>C r.(?) p.(Glu852Asp) - pathogenic g.2086858A>C g.2086858A>C - - SMARCA2_000014 - PubMed: Van Houdt et al 2012 - - Unknown - - - 0 - SIB - Livia Famiglietti
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