Full data view for gene DCC

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

4 entries on 1 page. Showing entries 1 - 4.
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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     

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VIP     

Data_av     

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Panel size     

Owner     
+?/. 8 c.1409G>A r.(?) p.(Gly470Val) FN3-1 Maternal (confirmed) ACMG likely benign g.50683873G>A g.53157503G>A - - DCC_000015 ACMG: PM1, PP4, BS1, BP4 - Likely benign PubMed: Meneret 2014 ClinVar-187790 rs141813053 Germline - ExAC 385 / 121006 - - - DNA SEQ, QMPSF Blood Quantitative Multiplex PCR of Short Fluorescent fragments ?, MRMV1 - PubMed: Meneret 2014 - F - Italy white - - - - 1 Ashley Marsh
+/+ - c.1409G>A r.(?) p.(Gly470Asp) - Maternal (inferred) - pathogenic g.50683873G>A g.53157503G>A - - DCC_000015 - - - - Germline - - - - - DNA SEQ-NG-I Blood - KAL, MRMV1 - PubMed: Bouilly 2018 Caucasian M no - - - - - - 1 Ashley Marsh
+/. - c.1409G>A r.(?) p.Gly470Asp - Unknown - NA g.50683873G>A g.53157503G>A - - DCC_000015 significantly decreased EGR1-promoter activation, impaired cytoskeletal and membrane rearrangement, CADD = D, GERP = 5.4 - - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.1409G>A r.(?) p.(Gly470Asp) - Unknown - VUS g.50683873G>A g.53157503G>A DCC(NM_005215.3):c.1409G>A (p.G470D) - DCC_000015 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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