All variants in the AGL gene

Information The variants shown are described using the NM_000642.2 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     
+?/. 25 c.3295T>C r.(3295u>c) p.(Trp1099Arg) - likely pathogenic g.100361877T>C g.99896321T>C - - AGL_000021 - - - - Germline/De novo (untested) yes - - 0 - François Petit
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