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.

4 entries on 1 page. Showing entries 1 - 4.
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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     
+/+ 7 c.924T>G r.(?) p.(Tyr308*) - Maternal (inferred) - pathogenic g.85212876A>C g.85957871A>C 954T>G - CHM_000050 hemizygous PubMed: van den Hurk 2003 - - Germline - - - - - DNA SEQ - - CHM - PubMed: van den Hurk 2003 - M - - - - - - - 1 David Baux
+?/. - c.924T>G r.(?) p.(Tyr308*) - Parent #1 - likely pathogenic g.85212876A>C g.85957871A>C CHM, variant 1: c.924T>G/p.Y308* - CHM_000050 solved, hemizygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ blood Sanger sequencing retinal disease 24 PubMed: Weisschuh 2020 Filing key number: 13, choroideremia, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.924T>G r.(?) p.(Tyr308*) - Parent #1 - likely pathogenic g.85212876A>C g.85957871A>C CHM, variant 1: c.924T>G/p.Y308* - CHM_000050 solved, hemizygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ blood Sanger sequencing retinal disease 25 PubMed: Weisschuh 2020 Filing key number: 13, choroideremia, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.924T>G r.(?) p.(Tyr308*) - Parent #1 - likely pathogenic g.85212876A>C g.85957871A>C CHM, variant 1: c.924T>G/p.Y308* - CHM_000050 solved, hemizygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ blood Sanger sequencing retinal disease 26 PubMed: Weisschuh 2020 Filing key number: 13, choroideremia, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
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