All variants in the IMPG1 gene

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

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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     

Owner     
-/. 1i_6i c.145-212_772-211insA r.spl? p.? - benign g.76728681_76751978insT - IVS2-212insA - IMPG1_000061 - PubMed: Abdel Aziz 2005 - - Germline - 16.5% (in 100 controls) - - - LOVD
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