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.

3 entries on 1 page. Showing entries 1 - 3.
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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     
-/. 18 c.2435A>C r.(?) p.(Tyr812Ser) kinase domain Unknown - benign g.112779920A>C g.112022343A>C - - MERTK_000099 reported in a patient with pathogenic mutation on RPGRIP; Align GVGD class C65; SIFT deleterious (score 0); Mutation Taster disease causing (p value=1); Polyphen2 probably damaging with a score of 1 (sensitivity: 0.00; specificity: 1.00) and conserved residue PubMed: Eisenberger 2013 - rs141361084 Germline - - - - - DNA SEQ - - LCA ? PubMed: Eisenberger 2013 - - - Saudi Arabia - - - - - 1 Isabelle Audo
?/. - c.2435A>C r.(?) p.(Tyr812Ser) - Unknown - VUS g.112779920A>C g.112022343A>C - - MERTK_000099 - PubMed: Wang 2014 - - Germline - - - - - DNA SEQ-NG - 66-gene panel retinal disease 10 PubMed: Wang 2014 - M - United States - - - - - 1 LOVD
+?/. 19 c.2435A>C r.(?) p.(Tyr812Ser) - Unknown - likely pathogenic g.112779920A>C - c.2435A>C - MERTK_000099 - PubMed: Eisenberger-2013 - rs141361084 Germline - - - - - DNA SEQ-NG-I, SEQ-NG-R, SEQ blood - retinal disease - PubMed: Eisenberger-2013 - M ? Saudi Arabia - - - - - 1 LOVD
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