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     
+/. 4 c.634A>C r.(?) p.(Thr212Pro) Ig-like C2 type 2 Parent #1 - pathogenic g.112705021A>C g.111947444A>C - - MERTK_000054 Align GVGD class C35; SIFT delerious (score 0); Mutation Taster disease causing (p value=0.997) Polyphen2 probably damaging with a score of 0.988 (sensitivity: 0.73; specificity: 0.96) and conserved residue Khan 2017 - - Germline - - - - - DNA SEQ - - ? ? Khan 2017 - - - United Kingdom (Great Britain) - - - - - 2 Isabelle Audo
+/. - c.634A>C r.(?) p.(Thr212Pro) - Parent #2 - pathogenic g.112705021A>C g.111947444A>C - - MERTK_000054 - PubMed: Khan 2017 - - Germline - - - - - DNA SEQ-NG - 105-gene panel retinal disease 3259 PubMed: Khan 2017 see paper - - United Kingdom (Great Britain) - - - - - 1 LOVD
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