All variants in the AGL gene

Information The variants shown are described using the NM_000642.2 transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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.2390A>G r.(?) p.(Asn797Ser) - likely benign g.100349757A>G g.99884201A>G AGL(NM_000028.2):c.2390A>G (p.(Asn797Ser)) - AGL_000037 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
?/. - c.2390A>G r.(?) p.(Asn797Ser) - VUS g.100349757A>G g.99884201A>G - - AGL_000037 2 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs149210307 Germline - 2/2792 individuals - 0 - Mohammed Faruq
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