Full data view for gene MERTK

This database is one of the "Eye disease" gene variant databases.
Information The variants shown are described using the NM_006343.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

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     
+/. - c.1988_1989insAT r.(?) p.(Ile664Serfs*7) - Unknown ACMG pathogenic g.112767552_112767553insAT g.112009975_112009976insAT MERTK c.296_297del(;)1988_1989insAT, V1: c.1988_1989insAT, (p.Ile664SerfsTer7) - MERTK_000207 alleles in cis or trans; heterozygous PubMed: Chen 2021 - - Unknown ? - - - - DNA SEQ-NG blood 212 inherited retinal disease-related genes retinal disease F285 PubMed: Chen 2021 - ? - Taiwan - - - - - 1 LOVD
+/. - c.1988_1989insAT r.(?) p.(Ile664SerfsTer7) - Unknown - pathogenic g.112767552_112767553insAT g.112009975_112009976insAT MERTK c.296_297del(;)1988_1989insAT; p.(Ile664SerfsTer7) - MERTK_000207 heterozygous PubMed: Chen 2021 - - Germline/De novo (untested) ? Taiwan Biobank: 0; GnomAD_exome_East: 0; GnomAD_All: 0 - - - DNA SEQ-NG - targeted 212 IRD-related genes retinal disease F285 PubMed: Chen 2021 - - - Taiwan - - - - - 1 LOVD
Legend   How to query  


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.