Full data view for gene SERPING1

Information The variants shown are described using the NM_000062.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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+/+ 5 c.816_818del r.(?) p.(Asn272del) Unknown ACMG likely pathogenic g.57373613_57373615del g.57606140_57606142del 8455_8457delCAA - SERPING1_000161 Nomenclature: Variant is also known as c.813_815delCAA. The HGVS notation prescibed that on the forward strand it should be CAA at position c.816_818. Recurrent variant. In frame deletion; p.(Asn272del) affects a N-glycosylation site; the protein sequence for the Asn272 glycosylation site is NN(272)KIS. Asn272 deletion disrupts the recognition site, thereby altering protein folding and function; thus Asn272del is deleterious as demonstrated by cultured cells by Ren et al (2025). Asn250 is located at the end of helix F, close to Sheet 3A, with H-bonding with Ala245. Asn250 is a highly exposed residue within the shutter region. p.(Asn272del) is poorly biosynthesized in recombinant expression studies (Ren et al 2023), then classifying p.(Asn272del) within class II/III (ie., disturbed insertion of the RCL, conformational transition with spontaneous self or mutual insertion of the RCL). The c.816_818del variant in SERPING1 meets ACMG/ClinGen criteria to be classified as likely pathogenic: PP4_Str, PM4, PS4_Mod, PM2_Sup. Variant introduced in the Lund SERPING1 database http://structure.bmc.lu.se/idbase/SERPING1base/ Conflicting classifications of pathogenicity. Variant introduced in ClinVar as VUS by InVitae, San Francisco CA and as likely pathogenic by Research Centre For Medical Genetics, Moscow Russia PubMed: Bissler 1994 Journal: Roche 2005 Journal: Gösswein 2008 Journal: Lopez-Lera 2011 Journal: Xu 2012 Journal: Pedrosa 2016 Journal: Ponard 2019 Journal: Liu 2019 Journal: Ren 2023 Journal: Grover 2023 Journal: Ren 2025 ClinVar-SCV003439867 rs2495440974 Germline yes - - - - DNA SEQ blood - HAE1;HAE2 - Journal: Ren 2023 Recurrent variant. Carrying families in France, United States, Italy, Spain, China. - no - - - - - - 14 Christian Drouet
+/+ 5 c.816_818del r.(?) p.(Asn272del) Unknown ACMG likely pathogenic g.57373613_57373615del g.57606140_57606142del - - SERPING1_000161 In frame deletion. Variant affecting one of the three glycosylation sites of the serpin domain. Prone to oligomerization/latentisation. In frame deletion; p.(Asn272del) affects a N-glycosylation site; the protein sequence for the Asn272 glycosylation site is NN(272)KIS. Asn272 deletion disrupts the recognition site, thereby altering protein folding and function; thus Asn272del is deleterious with a poorly biosynthesized product in recombinant expression studies (Ren 2023), then classifying p.(Asn272del) within class II/III (ie., disturbed insertion of the RCL, conformational transition with spontaneous self or mutual insertion of the RCL). Asn250 is located at the end of helix F, close to Sheet 3A, with H-bonding with Ala245. Asn250 is a highly exposed residue within the shutter region. The c.816_818del variant in SERPING1 meets ACMG/ClinGen SVI guidance criteria to be classified as likely pathogenic: PP4_Str, PM4, PS4_Mod, PM2_Sup. Journal: Loli-Ausejo 2021 Journal: Wang 2022 ClinVar-SCV005200126.1 rs2495440974 Germline yes - - - - DNA SEQ blood - HAE1;HAE2 - - Recurrent variant, shown to be carried by multiple families Family 1, Spain (n=3) Family 2, China (n=2) Family 3,Russia - - Spain - - - - - 6 Christian Drouet
+/+ 5 c.816_818del r.(?) p.(Asn272del) Parent #1 ACMG pathogenic g.57373613_57373615del g.57606140_57606142del [-100C>G;816_818del] - SERPING1_000161 c.816_818del is a recurrent variant; Asn272 is a N-glycosylation site. Variant introduced in the Lund SERPING1 database http://structure.bmc.lu.se/idbase/SERPING1base/ PubMed: Verpy 1996 - - Germline ? - - - - DNA SEQ blood - HAE1;HAE2 - - - - - France - - - - - 1 Christian Drouet
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