Full data view for gene COMP

Information The variants shown are described using the NM_000095.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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     
+/? 9 c.950A>G r.(?) p.(Asp317Gly) Parent #1 - pathogenic g.18899046T>C g.18788237T>C - - COMP_000125 conserved functional residue in C-type motif; normal 2nd chromosome - - - Unknown - - - - - DNA SEQ - - EDM1 - - - - - - - - - - - 1 Michael Briggs
+?/. - c.950A>G r.(?) p.(Asp317Gly) Unknown - likely pathogenic g.18899046T>C g.18788237T>C - - COMP_000125 - PubMed: Jacob 2025 SUB14119515 - Germline/De novo (untested) - - - - - DNA SEQ, SEQ-NG - - skeletal dysplasia - PubMed: Jacob 2025 2-generation family, affected brother/sister, unaffected parents F;M - India - - - - - 2 Johan den Dunnen
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