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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 6 c.715C>T r.(?) p.(Arg239*) - Maternal (inferred) - pathogenic g.85213970G>A g.85958965G>A 745C>T - CHM_000037 hemizygous PubMed: Mc Taggart 2002 - - Germline - - -TaqI ; -XhoI - - DNA SEQ - - CHM - PubMed: Mc Taggart 2002 - M - - - - - - - 1 David Baux
+/+ 6 c.715C>T r.(?) p.(Arg239*) - Maternal (inferred) - pathogenic g.85213970G>A g.85958965G>A 745C>T - CHM_000037 hemizygous PubMed: van den Hurk 2003 - - Germline - - -TaqI ; -XhoI - - DNA SEQ - - CHM - PubMed: van den Hurk 2003 - M - - - - - - - 1 David Baux
+/+ 6 c.715C>T r.(?) p.(Arg239*) - Maternal (inferred) - pathogenic g.85213970G>A g.85958965G>A 745C>T - CHM_000037 hemizygous PubMed: Garcia-Hoyos 2008 - - Germline - - -TaqI ; -XhoI - - DNA SEQ - - CHM - PubMed: GarciajalopezHoyos 2008 - M - Spain - - - - - 1 David Baux
+/+ 6 c.715C>T r.(?) p.(Arg239*) - Unknown - pathogenic g.85213970G>A g.85958965G>A 745C>T - CHM_000037 hemizygous PubMed: Aleman TS 2017 - - Germline - - -TaqI ; -XhoI - - DNA SEQ - - CHM - PubMed: Aleman TS 2017 - - - - - - - - - 1 David Baux
+/. 6 c.715C>T r.(?) p.(Arg239*) - Maternal (inferred) - pathogenic g.85213970G>A g.85958965G>A - - CHM_000037 - - - - Germline - - - - - DNA SEQ - - CHM - - eyeGENE Participant F - United States - - - - - 1 Kerry Goetz
+/. 6 c.715C>T r.(?) p.(Arg239*) - Maternal (inferred) - pathogenic g.85213970G>A g.85958965G>A - - CHM_000037 - - - - Germline - - - - - DNA SEQ - - CHM - - eyeGENE Participant, also 3Y9+9.69, 3Y9+9.99, 4XG+Q.43, 5J6+L.50, M - United States - - - - - 5 Kerry Goetz
+/. 6 c.715C>T r.(?) p.(Arg239*) - Unknown ACMG pathogenic g.85213970G>A - - - CHM_000037 - PubMed: Sharon 2019 - - Germline - 2/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 2 IRD families - - Israel - - - - - 2 Global Variome, with Curator vacancy
+/. - c.715C>T r.(?) p.(Arg239*) - Maternal (confirmed) - pathogenic (recessive) g.85213970G>A - - - CHM_000037 - PubMed: de Castro-Miro 2018 - - Germline yes - - - - DNA SEQ, SEQ-NG - WES retinal disease Fam50ORG PubMed: de CastrojalopezMiro 2018 4-generation family, 4 affected males M - Spain - - - - - 5 Johan den Dunnen
+?/. - c.715C>T r.(?) p.(Arg239*) - Unknown ACMG pathogenic g.85213970G>A - - - CHM_000037 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - CHM IR_GS_0086 - - M - Korea, South (Republic) - - - - - 1 Jinu Han
+?/. - c.715C>T r.(?) p.(Arg239*) - Parent #1 - likely pathogenic g.85213970G>A g.85958965G>A CHM, variant 1: c.715C>T/p.R239* - CHM_000037 solved, hemizygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ blood Sanger sequencing retinal disease 233 PubMed: Weisschuh 2020 Filing key number: 81, choroideremia, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. 6 c.715C>T r.(?) p.(Arg239*) - Maternal (inferred) - pathogenic g.85213970G>A - c.715C>T - CHM_000037 - PubMed: McLaren 2020 - - De novo no - - - - DNA SEQ - Sanger sequencing of CHM retinal disease - PubMed: McLaren 2020 Proband M - Australia Australian - - - - 1 LOVD
+?/. 6 c.715C>T r.(?) p.(Arg239*) - Maternal (inferred) - likely pathogenic g.85213970G>A - c.715C>T - CHM_000037 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 49 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+?/. 6 c.715C>T r.(?) p.(Arg239*) - Maternal (inferred) - likely pathogenic g.85213970G>A - c.715C>T - CHM_000037 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 50 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+?/. 6 c.715C>T r.(?) p.(Arg239*) - Maternal (inferred) - likely pathogenic g.85213970G>A - c.715C>T - CHM_000037 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 55 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+?/. 6 c.715C>T r.(?) p.(Arg239*) - Maternal (inferred) - likely pathogenic g.85213970G>A - c.715C>T - CHM_000037 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 56 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+?/. 6 c.715C>T r.(?) p.(Arg239*) - Maternal (inferred) - likely pathogenic g.85213970G>A - c.715C>T - CHM_000037 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 60 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+/. - c.715C>T r.(?) p.(Arg239*) - Unknown - pathogenic g.85213970G>A - CHM(NM_001362517.1):c.271C>T (p.R91*) - CHM_000037 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.715C>T r.(?) p.(Arg239Ter) - Unknown ACMG pathogenic (dominant) g.85213970G>A g.85958965G>A - - CHM_000037 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 - - Germline/De novo (untested) - - - - - DNA SEQ-NG - WGS ? SRP-1220 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
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