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.
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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     
+?/. 1i_10i c.-8162_1145-1212del r.spl? p.? - Unknown - likely pathogenic g.112648151_112739207del - c.-8162_1145-1212del, p.? - MERTK_000209 - PubMed: Jonsson 2018 - - Germline - - - - - DNA, RNA PE, SEQ-NG, RT-PCR, SEQ blood - retinal disease RP115 PubMed: Jonsson 2018 novel heterozygous variant in the MER proto-oncogene, tyrosine kinase F - - Sweden - - - - 1 LOVD
+?/. 1i_10i c.-8162_1145-1212del r.spl? p.? - Unknown - likely pathogenic g.112648151_112739207del - c.-8162_1145-1212del, p.? - MERTK_000209 - PubMed: Jonsson 2018 - - Germline - - - - - DNA, RNA PE, SEQ-NG, RT-PCR, SEQ blood - retinal disease RP116 PubMed: Jonsson 2018 novel heterozygous variant in the MER proto-oncogene, tyrosine kinase M - - Sweden - - - - 1 LOVD
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