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.

7 entries on 1 page. Showing entries 1 - 7.
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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     
?/. 2i c.116+80C>T r.(?) p.(=) - Unknown - VUS g.85282415G>A g.86027411G>A - - CHM_000161 - 1015148 - - Germline - - - - - DNA SEQ - - ? - 1015148 eyeGENE participant M - United States - - - - - 1 Kerry Goetz
?/. 2i c.116+80C>T r.(?) p.(=) - Unknown - VUS g.85282415G>A g.86027411G>A - - CHM_000161 - 1015148 - - Germline - - - - - DNA SEQ - - CHM - - and HM+C.46, N7+C.34, NE+W.26, NE+W.41, QU+U.10, eyeGENE participants M - United States - - - - - 6 Kerry Goetz
?/. 2i c.116+80C>T r.(?) p.(=) - Unknown - VUS g.85282415G>A g.86027411G>A - - CHM_000161 - - - - Germline - - - - - DNA SEQ - - BCD - - eyeGENE participant F - United States - - - - - 1 Kerry Goetz
?/. 2i c.116+80C>T r.(?) p.(=) - Unknown - VUS g.85282415G>A g.86027411G>A - - CHM_000161 - - - - Germline - - - - - DNA SEQ - - ? - - eyeGENE participant F - United States - - - - - 1 Kerry Goetz
?/. 2i c.116+80C>T r.(?) p.(=) - Unknown - VUS g.85282415G>A g.86027411G>A - - CHM_000161 - - - - Germline - - - - - DNA SEQ - - CHM - - eyeGENE participant F - United States - - - - - 1 Kerry Goetz
-?/. 2i c.116+80C>T r.(=) p.(=) - Maternal (inferred) - likely benign g.85282415G>A - c.116+80C>T - CHM_000161 - PubMed: Ouyang 2017 - rs1015148 Germline - - - - - DNA PCR, SEQ - - retinal disease - PubMed: Ouyang 2017 - M ? China - - - - - 1 LOVD
-?/. 2i c.116+80C>T r.(=) p.(=) - Unknown - likely benign g.85282415G>A - c.116+80C>T - CHM_000161 - PubMed: Ouyang 2017 - rs1015148 Germline - - - - - DNA PCR, SEQ - - retinal disease - PubMed: Ouyang 2017 - F ? China - - - - - 1 LOVD
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