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.

22 entries on 1 page. Showing entries 1 - 22.
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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     
+/+ 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - pathogenic g.85212923G>A g.85957918G>A 907C>T - CHM_000048 hemizygous; REP-1 not detected PubMed: van den Hurk 2003 - - Germline - - - - - DNA SEQ - - CHM - PubMed: van den Hurk 2003 - M - - - - - - - 1 David Baux
+/+ 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - pathogenic g.85212923G>A g.85957918G>A 907C>T - CHM_000048 hemizygous; REP-1 not detected PubMed: van den Hurk 2003 - - Germline - - - - - DNA SEQ - - CHM - PubMed: van den Hurk 2003 - M - - - - - - - 1 David Baux
+/+ 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - pathogenic g.85212923G>A g.85957918G>A 907C>T - CHM_000048 hemizygous; REP-1 not detected PubMed: van den Hurk 2003 - - Germline - - - - - DNA SEQ - - CHM - PubMed: van den Hurk 2003 - M - - - - - - - 1 David Baux
+/+ 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - pathogenic g.85212923G>A g.85957918G>A 907C>T - CHM_000048 hemizygous; REP-1 not detected PubMed: van den Hurk 2003 - - Germline - - - - - DNA SEQ - - CHM - PubMed: van den Hurk 2003 - M - - - - - - - 1 David Baux
+/+ 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - pathogenic g.85212923G>A g.85957918G>A 907C>T - CHM_000048 hemizygous; REP-1 not detected PubMed: Garcia-Hoyos 2008 - - Germline - - - - - DNA SEQ - - CHM - PubMed: GarciajalopezHoyos 2008 - M - Spain - - - - - 1 David Baux
+/+ 7 c.877C>T r.877c>u p.Arg293* - Maternal (confirmed) - pathogenic g.85212923G>A g.85957918G>A 907C>T - CHM_000048 hemizygous PubMed: Esposito 2011 - - Germline - - - - - DNA, RNA, protein PCR, PTT, RT-PCR, SEQ - - CHM - PubMed: Esposito 2011 - M - Italy - - - - - 1 Francesco Salvatore
+/+ 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - pathogenic g.85212923G>A g.85957918G>A 907C>T - CHM_000048 hemizygous; REP-1 not detected PubMed: van Bokhoven 1994 - - Germline - - - - - DNA SEQ - - CHM - PubMed: van Bokhoven 1994 - M - Denmark - - - - - 1 David Baux
+/+ 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - pathogenic g.85212923G>A g.85957918G>A 907C>T - CHM_000048 hemizygous; REP-1 not detected PubMed: Mc Donald 1998 - - Germline - - - - - DNA SEQ - - CHM - PubMed: Mc Donald 1998 - M - - - - - - - 1 David Baux
+/. 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - pathogenic g.85212923G>A g.85957918G>A - - CHM_000048 - - - - Germline - - - - - DNA SEQ - - CHM - - eyeGENE Participant, also UGH+K.24, M - United States - - - - - 2 Kerry Goetz
+/. 7 c.877C>T r.(?) p.(Arg293*) - Unknown ACMG pathogenic g.85212923G>A - - - CHM_000048 - 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.877C>T r.(?) p.(Arg293*) - Unknown - likely pathogenic g.85212923G>A g.85957918G>A - - CHM_000048 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 934 PubMed: Stone 2017 1 affected M - (United States) - - - - - 1 LOVD
+?/. - c.877C>T r.(?) p.(Arg293*) - Parent #1 - likely pathogenic g.85212923G>A g.85957918G>A CHM, variant 1: c.877C>T/p.R293* - CHM_000048 solved, hemizygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ blood Sanger sequencing retinal disease 114 PubMed: Weisschuh 2020 Filing key number: 51, choroideremia, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - likely pathogenic (maternal) g.85212923G>A - c.877C>T - CHM_000048 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Liujalopez2020 - M - - - - - - - 1 LOVD
+?/. 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - likely pathogenic (maternal) g.85212923G>A - c.877C>T - CHM_000048 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Liujalopez2020 - M - - - - - - - 1 LOVD
+?/. 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - likely pathogenic (maternal) g.85212923G>A - c.877C>T - CHM_000048 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Liujalopez2020 - M - - - - - - - 1 LOVD
+/. 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - pathogenic g.85212923G>A - c.877C>T - CHM_000048 - PubMed: Gao 2020 - - Germline - - - - - DNA SEQ-NG blood - retinal disease - PubMed: Gao 2020 van Bokhoven H, 19994. Jolly JK, 2015. M ? China - - - - - 1 LOVD
+?/. 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - likely pathogenic g.85212923G>A - c.877C>T - CHM_000048 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 53 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+?/. 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - likely pathogenic g.85212923G>A - c.877C>T - CHM_000048 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 54 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+?/. 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - likely pathogenic g.85212923G>A - c.877C>T - CHM_000048 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 59 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+?/. 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - likely pathogenic g.85212923G>A - c.877C>T - CHM_000048 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 62 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+?/. 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - likely pathogenic g.85212923G>A - c.877C>T - CHM_000048 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 63 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+?/. 7 c.877C>T r.(?) p.(Arg293*) - Maternal (inferred) - likely pathogenic g.85212923G>A - c.877C>T - CHM_000048 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 64 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
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