Full data view for gene DCC

Information The variants shown are described using the NM_005215.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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     
?/+? 4 c.817T>C r.(?) p.(Trp273Arg) IgC2-3 Maternal (confirmed) ACMG VUS g.50450196T>C g.52923826T>C - - DCC_000032 ACMG criteria - PM1, PM2, PP1, PP3, PP4 Likely pathogenic PubMed: Bierhals 2018 - - Germline yes - - - - DNA SEQ Blood - MRMV1 P3a PubMed: Bierhals 2018 - F no Germany white - - - - 3 Tatjana Bierhals
?/. 4 c.817T>C r.(?) p.Trp273Arg - Unknown - NA g.50450196T>C g.52923826T>C - - DCC_000032 CADD - 26.7, REVEL - 0.902, M-CAP - 0.624, MPC - 1.00 PubMed: Bierhals 2018 - - In silico - - - - - - - - - - - - - - - - - - - - - - -
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