Full data view for gene IMPG1

Information The variants shown are described using the NM_001563.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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VIP     

Methylation     

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Disease     

ID_report     

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Owner     
+/. - c.378G>A r.(?) p.(Trp126*) Unknown - pathogenic g.76744428C>T g.76034711C>T CNGB3: c.[1208G>A];[(1208G>A)], p.[R403Q];[(R403Q)], CNGA3: c.[1777G>A];[=], p.[E593K];[=], IMPG1: c.[378C>T];[=] (wrror in annotation, this protein truncation is caused by 378G>A), p.[W126*];[=] - IMPG1_000067 - PubMed: Burkhard 2018 - - Germline yes - - - - DNA SEQ-NG, SEQ blood - retinal disease 9 PubMed: Burkhard 2018 - F no - - - - - - 1 LOVD
+?/. - c.378G>A r.(?) p.(Trp126*) Parent #1 - likely pathogenic g.76744428C>T g.76034711C>T IMPG1, variant 1: c.378G>A/p.W126* - IMPG1_000067 solved, heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 830 PubMed: Weisschuh 2020 Filing key number: 342, macular dystrophy, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
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