Full data view for gene PLG

Information The variants shown are described using the NM_000301.3 transcript reference sequence.

5 entries on 1 page. Showing entries 1 - 5.
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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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Disease     

ID_report     

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?/. - c.112A>G r.(?) p.(Lys38Glu) Unknown - VUS g.161127501A>G g.160706469A>G PLG(NM_000301.3):c.112A>G (p.K38E), PLG(NM_000301.5):c.112A>G (p.K38E) - PLG_000017 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.112A>G r.(?) p.(Lys38Glu) Unknown - pathogenic g.161127501A>G g.160706469A>G PLG(NM_000301.3):c.112A>G (p.K38E), PLG(NM_000301.5):c.112A>G (p.K38E) - PLG_000017 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.112A>G r.(?) p.(Lys38Glu) Unknown - VUS g.161127501A>G g.160706469A>G PLG(NM_000301.3):c.112A>G (p.K38E), PLG(NM_000301.5):c.112A>G (p.K38E) - PLG_000017 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 2 c.112A>G r.(?) p.(Lys38Glu) Both (homozygous) ACMG pathogenic (recessive) g.161127501A>G g.160706469A>G K19E - PLG_000017 tPA-mediated activation assays could predict the clinical outcome for Lys38Glu carriers, but fibrin-independent uPA-mediated assays could not: p.Lys38Glu variant is likely not to be able to efficiently engage fibrin, with a subsequent short half-life. Lys19 is a very conserved residue among primates. One possible mechanism for plasminogen deficiency resulting from Lys to Glu substitution could be its location in the N-terminus region. In Glu1-PLG, p.Lys38Glu variant may lead to a relaxed conformational state, which is easier to activate and degrade. Journal: Tefs 2006 Journal: Bourrienne 2020 ClinVar-RCV000014551.38 rs73015965 Germline yes 0.00282 - - - DNA SEQ blood - deficiency, plasminogen, type I - Journal: Tefs 2006 Five independent families with homozygous affected patients have been shown as carrying a c.112A>G variant. Heterozygous carriers of these 5 families are not affected. Three independent families with compound heterozygous affected patients have been shown as carrying both c.112A>G and c.1468C>T variants. - - - - - - - - 8 Christian Drouet
+?/+? 2 c.112A>G r.(?) p.(Lys38Glu) Parent #1 ACMG pathogenic (recessive) g.161127501A>G g.160706469A>G - - PLG_000017 Variants c.112A>G and c.1468C>T have been found carried by compound heterozygous affected patients Journal: Tefs 2006 ClinVar-RCV000014551.38 rs73015965 Germline yes 0.00282 - - - DNA ? blood - deficiency, plasminogen, type I - Journal: Tefs 2006 Five independent families with homozygous affected patients have been shown as carrying a c.112A>G variant. Heterozygous carriers of these 5 families are not affected. Three independent families with compound heterozygous affected patients have been shown as carrying both c.112A>G and c.1468C>T variants. - - - - - - - - 8 Christian Drouet
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