All variants in the ALG9 gene

Information The variants shown are described using the NM_024740.2 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.1605T>G - p.? - likely benign g.111680496A>C g.111809772A>C - - ALG9_000020 14 heterozygous, no homozygous; Clinindb (India) Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message. PubMed: Narang 2020, Journal: Narang 2020 - rs12575909 Germline - 14/2794 individuals - 0 - Mohammed Faruq
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