Full data view for gene USH2A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_206933.2 transcript reference sequence.

10 entries on 1 page. Showing entries 1 - 10.
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Effect     

Exon     

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Owner     
+?/? 26 c.5200G>C r.(?) p.(Gly1734Arg) Laminin G-like 2 (1714-1891) Parent #1 ACMG VUS g.216256896C>G g.216083554C>G - - USH2A_000382 Heterozygous PubMed: Liu 2010, USMA missense analysis, missense variant in MSV3d - - Germline - 0/100 controls -NlaIII - - DNA SEQ - - USH2 - PubMed: Liu 2010 Relative M - China - - - - - 1 Anne-Françoise Roux
+?/? 26 c.5200G>C r.(?) p.(Gly1734Arg) Laminin G-like 2 (1714-1891) Parent #1 ACMG VUS g.216256896C>G g.216083554C>G - - USH2A_000382 Heterozygous PubMed: Liu 2010, USMA missense analysis, missense variant in MSV3d - - Germline - 0/100 controls -NlaIII - - DNA SEQ - - USH2 - PubMed: Liu 2010 Relative F - China - - - - - 1 Anne-Françoise Roux
+?/? 26 c.5200G>C r.(?) p.(Gly1734Arg) Laminin G-like 2 (1714-1891) Parent #1 ACMG VUS g.216256896C>G g.216083554C>G - - USH2A_000382 Heterozygous PubMed: Liu 2010, USMA missense analysis, missense variant in MSV3d - - Germline - 0/100 controls -NlaIII - - DNA SEQ - - USH2 - PubMed: Liu 2010 Proband F - China - - - - - 1 Anne-Françoise Roux
+/+ 26 c.5200G>C r.(?) p.(Gly1734Arg) Laminin G-like 2 (1714-1891) Paternal (inferred) ACMG VUS g.216256896C>G g.216083554C>G - - USH2A_000382 Homozygous PubMed: Liu 2010, USMA missense analysis, missense variant in MSV3d - - Germline - 0/100 controls -NlaIII - - DNA SEQ - - RPar - PubMed: Liu 2010 Proband M - China - - - - - 1 Anne-Françoise Roux
+/+ 26 c.5200G>C r.(?) p.(Gly1734Arg) Laminin G-like 2 (1714-1891) Maternal (inferred) ACMG VUS g.216256896C>G g.216083554C>G - - USH2A_000382 Homozygous PubMed: Liu 2010, USMA missense analysis, missense variant in MSV3d - - Germline - 0/100 controls -NlaIII - - DNA SEQ - - RPar - PubMed: Liu 2010 Proband M - China - - - - - 1 Anne-Françoise Roux
+?/? 26 c.5200G>C r.(?) p.(Gly1734Arg) Laminin G-like 2 (1714-1891) Parent #2 ACMG VUS g.216256896C>G g.216083554C>G - - USH2A_000382 Heterozygous; mutation PubMed: Jiang 2015, USMA missense analysis, missense variant in MSV3d - - Germline - - -NlaIII - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Jiang 2015 Proband F - China - - - - - 1 Anne-Françoise Roux
+?/. 26 c.5200G>C r.(?) p.(Gly1734Arg) - Unknown - likely pathogenic (recessive) g.216256896C>G - c.5200G>C - USH2A_000382 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - M - - - - - - - 1 LOVD
+/. - c.5200G>C r.(?) p.(Gly1734Arg) - Parent #2 - pathogenic g.216256896C>G g.216083554C>G USH2A c.5200G>C, p.Gly1734Arg - USH2A_000382 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD16100083 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+?/. 26 c.5200G>C r.(?) p.(Gly1734Arg) - Parent #2 ACMG likely pathogenic g.216256896C>G g.216083554C>G USH2A c.5200G>C, p.G1734R - USH2A_000382 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease USHsrf48 PubMed: Zhu 2021 family 209, patient USHsrf48 F - China - - - - - 1 LOVD
+?/. - c.5200G>C r.(?) p.(Gly1734Arg) - Unknown ACMG likely pathogenic g.216256896C>G g.216083554C>G - - USH2A_000382 ACMG GN005 criteria: PM2_P PM3_S PP1_M PubMed: Gao, F. J. et al., 2021; PubMed: Liu, X. et al., 2010; PubMed: Jiang, L. et al., 2015 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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