Full data view for gene CHM


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_000390.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

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     
+?/+ 1 c.3G>A r.3g>a p.0? - Maternal (inferred) ACMG likely pathogenic g.85302534C>T g.86047530C>T 33G>A - CHM_000128 hemizygous PubMed: Strunnikova 2009 - - Germline - - -BccI;-EciI; - - DNA, RNA, protein SEQ - - CHM - PubMed: Strunnikova 2009 Proband M - - - - - - - 1 Anne-Françoise Roux
+/. 1 c.3G>A r.(?) p.0? - Maternal (inferred) - pathogenic g.85302534C>T g.86047530C>T Met1? - CHM_000128 - - - - Germline - - - - - DNA SEQ - - CHM - - eyeGENE Participant M - United States - - - - - 1 Kerry Goetz
+?/. - c.3G>A r.(?) p.(Met1?) - Unknown ACMG likely pathogenic g.85302534C>T g.86047530C>T CHM c.3G>A, p.(Met1?) - CHM_000128 - PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 80 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
Legend   How to query  


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.