Full data view for gene DHX30

Information The variants shown are described using the NM_138615.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

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     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. - c.2345G>A r.(?) p.(Arg782Gln) Unknown - likely pathogenic g.47889728G>A g.47848238G>A - - DHX30_000011 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.2345G>A r.(?) p.(Arg782Gln) Unknown ACMG pathogenic g.47889728G>A - - - DHX30_000011 - - - - De novo yes - - - - DNA SEQ-NG - - NDD - - - M - - - - - - - 1 Davor Lessel
Legend   How to query