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.

6 entries on 1 page. Showing entries 1 - 6.
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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     
+/+ _1_1i c.-30_(49+1_50-1){0} r.0 p.0 - Maternal (inferred) - pathogenic g.(85282562_85302487)_(85302566_?)del g.(86027558_86047483)_(85302566_?)del 1-?_79+?del - CHM_000095 hemizygous; REP-1 not detected PubMed: Mc Taggart 2002 - - Germline - - - - - DNA SEQ - - CHM - PubMed: Mc Taggart 2002 - M - - - - - - - 1 David Baux
+/+ _1_1i c.-30_(49+1_50-1){0} r.0 p.0 - Maternal (inferred) - pathogenic g.(85282562_85302487)_(85302566_?)del g.(86027558_86047483)_(85302566_?)del 1-?_79+?del - CHM_000095 hemizygous; REP-1 not detected PubMed: Mc Taggart 2002 - - Germline - - - - - DNA SEQ - - CHM - PubMed: Mc Taggart 2002 - M - - - - - - - 1 David Baux
+/+ _1_1i c.-30_(49+1_50-1){0} r.0 p.0 - Unknown - pathogenic g.(85282562_85302487)_(85302566_?)del g.(86027558_86047483)_(85302566_?)del 1-?_79+?del - CHM_000095 heterozygous PubMed: Yau 2007 - - Germline - - - - - DNA SEQ - - CHM - PubMed: Yau 2007 Carrier F - - - - - - - 1 David Baux
?/? _1_1i c.-30_(49+1_50-1){0} r.0 p.0 - Unknown - VUS g.(85282562_85302487)_(85302566_?)del g.(86027558_86047483)_(85302566_?)del 1-?_79+?del - CHM_000095 heterozygous PubMed: Aleman TS 2017 - - Germline - - - - - DNA SEQ - - CHM - PubMed: Aleman TS 2017 - M - - - - - - - 1 David Baux
+/+ _1_1i c.-30_(49+1_50-1){0} r.0 p.0 - Maternal (inferred) - pathogenic g.(85282562_85302487)_(85302566_?)del g.(86027558_86047483)_(85302566_?)del 1-?_79+?del - CHM_000095 hemizygous PubMed: van den Hurk 1997 - - Germline - - - - - DNA SEQ - - CHM - PubMed: van den Hurk 1997 - M - - - - - - - 1 David Baux
+/+ _1_1i c.-30_(49+1_50-1){0} r.0 p.0 - Maternal (inferred) - pathogenic g.(85282562_85302487)_(85302566_?)del g.(86027558_86047483)_(85302566_?)del 1-?_79+?del - CHM_000095 hemizygous PubMed: van den Hurk 1997 - - Germline - - - - - DNA SEQ - - CHM - PubMed: van den Hurk 1997 - M - - - - - - - 1 David Baux
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