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.

10 entries on 1 page. Showing entries 1 - 10.
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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     
+/+ 2i c.116+1G>A r.spl p.? - Maternal (inferred) - pathogenic g.85282494C>T g.86027490C>T 146+1G>A - CHM_000009 hemizygous PubMed: Fujiki 1999 - - Germline - - - - - DNA SEQ - - CHM - PubMed: Fujiki 1999 - M - Japan - - - - - 1 David Baux
+/+ 2i c.116+1G>A r.spl p.? - Maternal (inferred) - pathogenic g.85282494C>T g.86027490C>T 146+1G>A - CHM_000009 hemizygous PubMed: Mc Taggart 2002 - - Germline - - - - - DNA SEQ - - CHM - PubMed: Mc Taggart 2002 - M - - - - - - - 1 David Baux
+/+ 2i c.116+1G>A r.spl p.? - Maternal (inferred) - pathogenic g.85282494C>T g.86027490C>T 146+1G>A - CHM_000009 hemizygous PubMed: van den Hurk 2003 - - Germline - - - - - DNA SEQ - - CHM - PubMed: van den Hurk 2003 - M - - - - - - - 1 David Baux
+/+ 2i c.116+1G>A r.spl p.? - Unknown - pathogenic g.85282494C>T g.86027490C>T 146+1G>A - CHM_000009 hemizygous PubMed: Aleman TS 2017 - - Germline - - - - - DNA SEQ - - CHM - PubMed: Aleman TS 2017 - - - - - - - - - 1 David Baux
+/. 2i c.116+1G>A r.spl p.(Gly17Glufs) - Maternal (inferred) - pathogenic g.85282494C>T g.86027490C>T - - CHM_000009 - - - - Germline - - - - - DNA SEQ - - CHM - - eyeGENE Participant M - United States - - - - - 1 Kerry Goetz
+/. - c.116+1G>A p.(?) p.? - Maternal (confirmed) ACMG pathogenic g.85282494C>T g.86027490C>T c.116+1G>A - CHM_000009 - PubMed: Zhang 2016 - - Germline - - - - - DNA SEQ-NG - 226-gene panel retinal disease BLM049 PubMed: Zhang 2016 family M - United States Hispanic - - - - 1 LOVD
+/. 2i c.116+1G>A r.spl? p.? - Maternal (inferred) - pathogenic g.85282494C>T - c.116+1G>A - CHM_000009 - PubMed: Vitale 2020 - - Unknown ? - - - - DNA arrayCGH, SEQ - - retinal disease - PubMed: Vitale 2020 - M ? United States - - - - - 1 LOVD
+/. 2i c.116+1G>A r.spl? p.? - Maternal (inferred) - pathogenic g.85282494C>T - c.116+1G>A - CHM_000009 - PubMed: Vitale 2020 - - Unknown ? - - - - DNA arrayCGH, SEQ - - retinal disease - PubMed: Vitale 2020 - M ? United States - - - - - 1 LOVD
+?/. 2i c.116+1G>A r.spl? p.? - Maternal (inferred) - likely pathogenic g.85282494C>T - c.116+1G>A - CHM_000009 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 77 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+/. - c.116+1G>A r.spl p.? - Parent #1 ACMG pathogenic (dominant) g.85282494C>T g.86027490C>T - - CHM_000009 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? CHM-15 PubMed: Weisschuh 2024 family, 2 affected F - Germany - - - - - 2 Johan den Dunnen
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