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     
?/. - c.791C>G r.(?) p.(Ala264Gly) - Unknown - VUS g.112722801C>G g.111965224C>G MERTK(NM_006343.2):c.791C>G (p.A264G) - MERTK_000014 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. 5 c.791C>G r.(?) p.(Ala264Gly) Ig-like C2 type 2 Parent #1 - benign g.112722801C>G g.111965224C>G - - MERTK_000014 reported in patient with two pathogenic variants in EYS; Align GVGD class C55; 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 - rs199779970 Germline - - - - - DNA SEQ-NG-I - - retinal disease - PubMed: Eisenberger 2014 - M no Austria - - - - - 1 Rob W.J. Collin
?/. - c.791C>G r.(?) p.(Ala264Gly) - Unknown - VUS g.112722801C>G g.111965224C>G - - MERTK_000014 - PubMed: Tiwari 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease Case71882 PubMed: Tiwari 2016 see paper M - Switzerland - - - - - 1 LOVD
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