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.

21 entries on 1 page. Showing entries 1 - 21.
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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.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - pathogenic g.85213886G>A g.85958881G>A 829C>T - CHM_000043 hemizygous PubMed: Fujiki 1999 - - Germline - - - TaqI - - DNA SEQ - - CHM - PubMed: Fujiki 1999 - M - Japan - - - - - 1 David Baux
+/+ 6 c.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - pathogenic g.85213886G>A g.85958881G>A 829C>T - CHM_000043 hemizygous PubMed: Fujiki 1999 - - Germline - - - TaqI - - DNA SEQ - - CHM - PubMed: Fujiki 1999 - M - Japan - - - - - 1 David Baux
+/+ 6 c.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - pathogenic g.85213886G>A g.85958881G>A 829C>T - CHM_000043 hemizygous PubMed: Fujiki 1999 - - Germline - - - TaqI - - DNA SEQ - - CHM - PubMed: Fujiki 1999 - M - Japan - - - - - 1 David Baux
+/+ 6 c.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - pathogenic g.85213886G>A g.85958881G>A 829C>T - CHM_000043 hemizygous PubMed: Mc Taggart 2002 - - Germline - - - TaqI - - DNA SEQ - - CHM - PubMed: Mc Taggart 2002 - M - - - - - - - 1 David Baux
+/+ 6 c.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - pathogenic g.85213886G>A g.85958881G>A 829C>T - CHM_000043 hemizygous PubMed: Mc Taggart 2002 - - Germline - - - TaqI - - DNA SEQ - - CHM - PubMed: Mc Taggart 2002 - M - - - - - - - 1 David Baux
+/+ 6 c.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - pathogenic g.85213886G>A g.85958881G>A 829C>T - CHM_000043 hemizygous PubMed: Mc Taggart 2002 - - Germline - - - TaqI - - DNA SEQ - - CHM - PubMed: Mc Taggart 2002 - M - - - - - - - 1 David Baux
+/+ 6 c.799C>T r.799c>u p.Arg267* - Maternal (confirmed) - pathogenic g.85213886G>A g.85958881G>A 829C>T - CHM_000043 hemizygous PubMed: Esposito 2011 - - Germline - - - TaqI - - DNA, RNA, protein PCR, PTT, RT-PCR, SEQ - - CHM - PubMed: Esposito 2011 de novo mutation in maternal germline M - Italy - - - - - 1 Francesco Salvatore
+/+ 6 c.799C>T r.(?) p.(Arg267*) - Unknown - pathogenic g.85213886G>A g.85958881G>A 829C>T - CHM_000043 hemizygous PubMed: Aleman TS 2017 - - Germline - - - TaqI - - DNA SEQ - - CHM - PubMed: Aleman TS 2017 - - - - - - - - - 1 David Baux
+/+ 6 c.799C>T r.(?) p.(Arg267*) - Unknown - pathogenic g.85213886G>A g.85958881G>A 829C>T - CHM_000043 hemizygous PubMed: Aleman TS 2017 - - Germline - - - TaqI - - DNA SEQ - - CHM - PubMed: Aleman TS 2017 - - - - - - - - - 1 David Baux
+/+ 6 c.799C>T r.(?) p.(Arg267*) - Unknown - pathogenic g.85213886G>A g.85958881G>A 829C>T - CHM_000043 hemizygous PubMed: Zhu L 2017 - - Germline - - - TaqI - - DNA SEQ - - CHM - PubMed: Zhu L 2017 - M - China - - - - - 1 David Baux
+/+ 6 c.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - pathogenic g.85213886G>A g.85958881G>A 829C>T - CHM_000043 hemizygous PubMed: van den Hurk 1997 - - Germline - - - TaqI - - DNA SSCA - - CHM - PubMed: van den Hurk 1997 - M - - - - - - - 1 David Baux
+/+ 6 c.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - pathogenic g.85213886G>A g.85958881G>A 829C>T - CHM_000043 hemizygous PubMed: Beaufrère 1997 - - Germline - - - TaqI - - DNA SEQ - - CHM - PubMed: Beaufrère 1997 - M - France - - - - - 1 David Baux
+/. 6 c.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - pathogenic g.85213886G>A g.85958881G>A - - CHM_000043 - - - - Germline - - - - - DNA SEQ - - CHM - - eyeGENE Participants, also 45Y+Y.77, QU+U.10, V56+S.66, , M - United States - - - - - 4 Kerry Goetz
+/. 6 c.799C>T r.(?) p.(Arg267*) - Unknown ACMG pathogenic g.85213886G>A - - - CHM_000043 - 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.799C>T r.(?) p.(Arg267*) - Unknown - likely pathogenic g.85213886G>A g.85958881G>A c.799G>A, p.(Arg267*) - CHM_000043 error in annotation: c.799G>A instead of C>T, hemizygous PubMed: Wang 2019 - - Germline ? - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 13014 PubMed: Wang 2019 - M - China - - - - - 1 LOVD
+/. 6 c.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - pathogenic g.85213886G>A - c.799C>T, p.Arg267* - CHM_000043 - PubMed: Vitale 2020 - - Unknown ? - - - - DNA arrayCGH, SEQ - - retinal disease - PubMed: Vitale 2020 - M ? United States - - - - - 1 LOVD
+/. 6 c.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - pathogenic g.85213886G>A - c.799C>T - CHM_000043 - PubMed: McLaren 2020 - - Germline yes - - - - DNA SEQ-NG - Targeted NGS of ocular genes (Retinal Dystrophy Panel v6, 226 genes) retinal disease - PubMed: McLaren 2020 Proband M - Australia Australian - - - - 1 LOVD
+/. 6 c.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - pathogenic g.85213886G>A - c.799C>T - CHM_000043 - PubMed: McLaren 2020 - - Germline yes - - - - DNA SEQ-NG - Targeted sequencing of familial CHM variant retinal disease - PubMed: McLaren 2020 Brother M - Australia Australian - - - - 1 LOVD
+/. 6 c.799C>T r.(?) p.(Arg267*) - Unknown - pathogenic g.85213886G>A - c.799C>T - CHM_000043 - PubMed: McLaren 2020 - - Germline yes - - - - DNA SEQ-NG - Targeted sequencing of familial CHM variant retinal disease - PubMed: McLaren 2020 Daughter: Obligate carrier F - Australia Australian - - - - 1 LOVD
+?/. 6 c.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - likely pathogenic g.85213886G>A - c.799C>T - CHM_000043 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 61 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
+?/. 6 c.799C>T r.(?) p.(Arg267*) - Maternal (inferred) - likely pathogenic g.85213886G>A - c.799C>T - CHM_000043 - PubMed: Dubis 2021 - - Germline - - - - - DNA SEQ blood - retinal disease 66 PubMed: Dubis 2021 - M - - Caucasian - - - - 1 LOVD
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