Full data view for gene ASAH1

This database is one of the gene variant databases from the "Leiden Muscular Dystrophy pages" (LMDp)
Information The variants shown are described using the transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

Methylation     

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Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.504A>C r.431_505del p.Glu145_Gly169del Parent #2 - pathogenic (recessive) g.17921967T>G g.18064458T>G - - ASAH1_000046 - PubMed: Kernohan 2017, PubMed: Fresard 2019 - - Germline - - - - - DNA, RNA RT-PCR, SEQ, SEQ-NG - WES SMA patient PubMed: Kernohan 2017, PubMed: Fresard 2019 - M no Canada - - - - - 1 Johan den Dunnen
+?/. - c.504A>C r.(?) p.(Lys168Asn) Maternal (confirmed) ACMG likely pathogenic g.17921967T>G - - - ASAH1_000046 ACMG PM1, PM2, PM3, PP4, PP5; The patient's electroclinical phenotype is consistent with previous reports of SMA-PME due to pathogenic variants in ASAH1. The parents are not related, consistent with the bi-allelic autosomal recessive inheritance of two rare damaging variants in this established PME gene. Thus, the phenotype is compatible with the genetic finding. PubMed: Courage 2021, Journal: Courage 2021 - - Germline yes - - - - DNA SEQ, SEQ-NG WES trio - SMAPME PME9 PubMed: Courage 2021, Journal: Courage 2021 - M no Australia - - - - - 1 Carolina Courage
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