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.

18 entries on 1 page. Showing entries 1 - 18.
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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     
+/+ 6 c.808C>T r.(?) p.(Arg270*) - Maternal (inferred) - pathogenic g.85213877G>A g.85958872G>A 838C>T - CHM_000044 hemizygous PubMed: Fujiki 1999 - - Germline - - +BtsCI;+FokI; - - DNA SEQ - - CHM - PubMed: Fujiki 1999 - M - Japan - - - - - 1 David Baux
+/+ 6 c.808C>T r.(?) p.(Arg270*) - Maternal (inferred) - pathogenic g.85213877G>A g.85958872G>A 838C>T - CHM_000044 hemizygous PubMed: Fujiki 1999 - - Germline - - +BtsCI;+FokI; - - DNA SEQ - - CHM - PubMed: Fujiki 1999 - M - Japan - - - - - 1 David Baux
+/+ 6 c.808C>T r.(?) p.(Arg270*) - Maternal (inferred) - pathogenic g.85213877G>A g.85958872G>A 838C>T - CHM_000044 hemizygous PubMed: van den Hurk 2003 - - Germline - - +BtsCI;+FokI; - - DNA SEQ - - CHM - PubMed: van den Hurk 2003 - M - - - - - - - 1 David Baux
+/+ 6 c.808C>T r.(?) p.(Arg270*) - Maternal (confirmed) - pathogenic g.85213877G>A g.85958872G>A - - CHM_000044 hemizygous PubMed: Perez-cano 2009 - - Germline - - +BtsCI;+FokI; - - DNA SEQ - - CHM - PubMed: Perezjalopezcano 2009 Proband M - Mexico - - - - - 1 Anne-Françoise Roux
+/+ 6 c.808C>T r.(?) p.(Arg270*) - Maternal (confirmed) - pathogenic g.85213877G>A g.85958872G>A 838C>T - CHM_000044 hemizygous PubMed: Perez-cano 2009 - - Germline - - +BtsCI;+FokI; - - DNA SEQ - - CHM - PubMed: Perezjalopezcano 2009 Relative M - Mexico - - - - - 1 Anne-Françoise Roux
+/+ 6 c.808C>T r.(?) p.(Arg270*) - Maternal (confirmed) - pathogenic g.85213877G>A g.85958872G>A 838C>T - CHM_000044 hemizygous PubMed: Perez-cano 2009 - - Germline - - +BtsCI;+FokI; - - DNA SEQ - - CHM - PubMed: Perezjalopezcano 2009 Relative - - Mexico - - - - - 1 Anne-Françoise Roux
+/+ 6 c.808C>T r.(?) p.(Arg270*) - Unknown - pathogenic g.85213877G>A g.85958872G>A 838C>T - CHM_000044 heterozygous PubMed: Perez-cano 2009 - - Germline - - +BtsCI;+FokI; - - DNA SEQ - - CHM - PubMed: Perezjalopezcano 2009 Carrier F - Mexico - - - - - 1 Anne-Françoise Roux
+/+ 6 c.808C>T r.(?) p.(Arg270*) - Unknown - pathogenic g.85213877G>A g.85958872G>A 838C>T - CHM_000044 hemizygous PubMed: Aleman TS 2017 - - Germline - - +BtsCI;+FokI; - - DNA SEQ - - CHM - PubMed: Aleman TS 2017 - M - - - - - - - 1 David Baux
+/. 6 c.808C>T r.(?) p.(Arg270*) - Maternal (inferred) - pathogenic g.85213877G>A g.85958872G>A - - CHM_000044 - - - - Germline - - - - - DNA SEQ - - CHM - - eyeGENE Participants, also N7+C.34, 53Z+5.67, VUT+V.85, , M - United States - - - - - 4 Kerry Goetz
+/. - c.808C>T r.(?) p.(Arg270*) - Parent #1 ACMG pathogenic g.85213877G>A g.85958872G>A - - CHM_000044 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19524 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+/. - c.808C>T r.(?) p.(Arg270*) - Parent #1 - pathogenic g.85213877G>A g.85958872G>A - - CHM_000044 - PubMed: Carrigan 2016 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease - PubMed: Carrigan 2016 - - - Ireland - - - - - 1 LOVD
?/. - c.808C>T r.(?) p.(Arg270Ter) - Parent #1 - VUS g.85213877G>A g.85958872G>A - - CHM_000044 - PubMed: Oishi 2014 - - Germline - - - - - DNA SEQ-NG - 193-gene panel retinal disease K1956 PubMed: Oishi 2014 family - - Japan - - - - - 1 LOVD
+?/. 6 c.808C>T r.(?) p.(Arg270*) - Maternal (inferred) - likely pathogenic (maternal) g.85213877G>A - c.808C>T - CHM_000044 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Liujalopez2020 - M - - - - - - - 1 LOVD
+?/. 6 c.808C>T r.(?) p.(Arg270*) - Maternal (inferred) - likely pathogenic (maternal) g.85213877G>A - c.808C>T - CHM_000044 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liujalopez2020 - M - - - - - - - 1 LOVD
+?/. 6 c.808C>T r.(?) p.(Arg270*) - Maternal (inferred) - likely pathogenic g.85213877G>A - c.808C>T - CHM_000044 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 68 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+?/. 6 c.808C>T r.(?) p.(Arg270*) - Maternal (inferred) - likely pathogenic g.85213877G>A - c.808C>T - CHM_000044 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 69 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+/. - c.808C>T r.(?) p.(Arg270Ter) - Parent #1 ACMG pathogenic (dominant) g.85213877G>A g.85958872G>A - - CHM_000044 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 143078 - Germline - - - - - DNA SEQ-NG - WGS ? CHM-112 PubMed: Weisschuh 2024 family, 2 affected M - Germany - - - - - 2 Johan den Dunnen
+/. - c.808C>T r.(?) p.(Arg270Ter) - Unknown - pathogenic g.85213877G>A - CHM(NM_001362517.1):c.364C>T (p.R122*) - CHM_000044 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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