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.

3 entries on 1 page. Showing entries 1 - 3.
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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     
+/+ 8 c.1019C>A r.(?) p.(Ser340*) - Maternal (inferred) - pathogenic g.85211305G>T g.85956300G>T 1049C>A - CHM_000056 hemizygous PubMed: Trujillo 1998 - - Germline - - - - - DNA SEQ - - CHM - PubMed: Trujillo 1998 - M - Spain - - - - - 1 David Baux
+/+ 8 c.1019C>A r.(?) p.(Ser340*) - Maternal (inferred) - pathogenic g.85211305G>T g.85956300G>T 1049C>A - CHM_000056 hemizygous PubMed: Mc Taggart 2002 - - Germline - - - - - DNA SEQ - - CHM - PubMed: Mc Taggart 2002 - M - - - - - - - 1 David Baux
+/+ 8 c.1019C>A r.(?) p.(Ser340*) - Maternal (inferred) - pathogenic g.85211305G>T g.85956300G>T 1049C>A - CHM_000056 hemizygous; REP-1 not detected PubMed: Yip 2007 - - Germline - - - - - DNA SEQ - - CHM - PubMed: Yip 2007 - M - China - - - - - 1 David Baux
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