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     
+/+ 8 c.1034C>G r.(?) p.(Ser345*) - Maternal (inferred) - pathogenic g.85211290G>C g.85956285G>C 1064C>G - CHM_000057 hemizygous PubMed: Fujiki 1999 - - Germline - - + NlaIII - - DNA SEQ - - CHM - PubMed: Fujiki 1999 - M - Japan - - - - - 1 David Baux
+/. 8 c.1034C>G r.(?) p.(Ser345*) - Unknown - pathogenic g.85211290G>C g.85956285G>C - - CHM_000057 - - - - Germline - - - - - DNA SEQ - - CHM - - eyeGENE Participant M - United States - - - - - 1 Kerry Goetz
+/. 8 c.1034C>G r.(?) p.(Ser345*) - Maternal (inferred) - pathogenic g.85211290G>C - c.1034C>G - CHM_000057 - PubMed: Hayashi 2020 - - Germline - - - - - DNA SEQ blood - retinal disease F7-JU0752 PubMed: Hayashi 2020 - M - Japan Japanese - - - - 1 LOVD
+/. 8 c.1034C>G r.(?) p.(Ser345*) - Maternal (inferred) - pathogenic g.85211290G>C - c.1034C>G - CHM_000057 - PubMed: Hayashi 2020 - - Germline - - - - - DNA SEQ blood - retinal disease F7-JU1817 PubMed: Hayashi 2020 - M - Japan Japanese - - - - 1 LOVD
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