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     
?/. - c.4331A>G r.(?) p.(Asn1444Ser) - VUS g.100382037A>G g.99916481A>G - - AGL_000073 conflicting interpretations of pathogenicity; 21 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs143815159 Germline - 21/2791 individuals - 0 - Mohammed Faruq
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