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.
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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     
+?/? 5 c.316C>T r.(?) p.(Gln106*) - Maternal (inferred) - likely pathogenic g.85219056G>A g.85964051G>A 346C>T - CHM_000020 hemizygous PubMed: Nesslinger 1996 - - Germline - - -Hpy188III - - DNA SEQ - - CHM - PubMed: Nesslinger 1996 - M - Canada - - - - - 1 David Baux
+/. 5 c.316C>T r.(?) p.(Gln106*) - Maternal (inferred) - pathogenic g.85219056G>A g.85964051G>A - - CHM_000020 - - - - Germline - - - - - DNA SEQ - - CHM - - eyeGENE Participant F - United States - - - - - 1 Kerry Goetz
+/. 5 c.316C>T r.(?) p.(Gln106*) - Maternal (confirmed) - pathogenic g.85219056G>A g.85964051G>A - - CHM_000020 - - - - Germline - - - - - DNA SEQ - - CHM - - eyeGENE Participant M - United States - - - - - 1 Kerry Goetz
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