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.

8 entries on 1 page. Showing entries 1 - 8.
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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     
+/+ 8 c.1138C>T r.(?) p.(Gln380*) - Maternal (inferred) - pathogenic g.85211186G>A g.85956181G>A 1168C>T - CHM_000059 hemizygous PubMed: Jacobson 2006 - - Germline - - - - - DNA SEQ - - CHM - PubMed: Jacobson 2006 - M - - - - - - - 1 David Baux
+/+ 8 c.1138C>T r.(?) p.(Gln380*) - Unknown - pathogenic g.85211186G>A g.85956181G>A 1168C>T - CHM_000059 hemizygous PubMed: Aleman TS 2017 - - Germline - - - - - DNA SEQ - - CHM - PubMed: Aleman TS 2017 - - - - - - - - - 1 David Baux
+/. 8 c.1138C>T r.(?) p.(Gln380*) - Unknown - pathogenic g.85211186G>A g.85956181G>A - - CHM_000059 - - - - Germline - - - - - DNA SEQ - - CHM - - eyeGENE Participants, K2+5.2, VYK+5.47, VUU+S.75 M - United States - - - - - 3 Kerry Goetz
+/. 8 c.1138C>T r.(?) p.(Gln380*) - Maternal (inferred) - pathogenic g.85211186G>A - c.1138C>T, p.Gln380* - CHM_000059 - PubMed: Vitale 2020 - - Unknown ? - - - - DNA arrayCGH, SEQ - - retinal disease - PubMed: Vitale 2020 - M ? United States - - - - - 1 LOVD
-?/. 8 c.1138C>T r.(?) p.(Gln380*) - Maternal (inferred) - likely benign g.85211186G>A - Gln380*C>T - CHM_000059 - PubMed: Vitale 2020 - - Unknown ? - - - - DNA arrayCGH, SEQ - - retinal disease - PubMed: Vitale 2020 had a mild CHM mutation but no visual complaints M ? United States - - - - - 1 LOVD
+/. 8 c.1138C>T r.(?) p.(Gln380*) - Maternal (inferred) - pathogenic g.85211186G>A - c.1138C>T, p.Gln380* - CHM_000059 - PubMed: Vitale 2020 - - Unknown ? - - - - DNA arrayCGH, SEQ - - retinal disease - PubMed: Vitale 2020 - M ? United States - - - - - 1 LOVD
+/. 8 c.1138C>T r.(?) p.(Gln380*) - Maternal (inferred) - pathogenic g.85211186G>A - c.1138C>T, p.Gln380* - CHM_000059 - PubMed: Vitale 2020 - - Unknown ? - - - - DNA arrayCGH, SEQ - - retinal disease - PubMed: Vitale 2020 - M ? United States - - - - - 1 LOVD
+/. 8 c.1138C>T r.(?) p.(Gln380*) - Maternal (inferred) - pathogenic g.85211186G>A - c.1138C>T, p.Gln380* - CHM_000059 - PubMed: Vitale 2020 - - Unknown ? - - - - DNA arrayCGH, SEQ - - retinal disease - PubMed: Vitale 2020 - M ? United States - - - - - 1 LOVD
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