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     

Predict/PolyPhen     

Predict/SIFT     

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     
+?/. 2 c.377C>A r.(?) p.(Ser126*) IgC2-1 - - Unknown - likely pathogenic g.50278709C>A g.52752339C>A - - DCC_000005 {CV:187794} PubMed: Meneret 2014 - - Germline - 0 - 0 - DNA SEQ, QMPSF Blood Quantitative Multiplex PCR of Short Fluorescent fragments ?, MRMV-1 - PubMed: Meneret 2014 - M - Germany Caucasian - 0 - - 1 Ashley Marsh
+?/. 2 c.377C>A r.(?) p.(Ser126*) IgC2-1 - - Paternal (confirmed) - likely pathogenic g.50278709C>A g.52752339C>A - - DCC_000005 {CV:187794} PubMed: Meneret 2014 - - Germline yes 0 - 0 - DNA SEQ, QMPSF Blood Quantitative Multiplex PCR of Short Fluorescent fragments ?, MRMV-1 - PubMed: Meneret 2014 - M - Germany Caucasian - 0 - - 1 Ashley Marsh
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