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.

7 entries on 1 page. Showing entries 1 - 7.
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+/+ 25 c.5167G>C r.(?) p.(Gly1723Arg) Laminin G-like 2 (1714-1891) Maternal (confirmed) - pathogenic g.216258040C>G g.216084698C>G - - USH2A_000287 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 25 c.5167G>C r.(?) p.(Gly1723Arg) Laminin G-like 2 (1714-1891) Paternal (confirmed) - pathogenic g.216258040C>G g.216084698C>G - - USH2A_000287 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 25 c.5167G>C r.(?) p.(Gly1723Arg) Laminin G-like 2 (1714-1891) Maternal (confirmed) - pathogenic g.216258040C>G g.216084698C>G - - USH2A_000287 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH3 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 25 c.5167G>C r.(?) p.(Gly1723Arg) Laminin G-like 2 (1714-1891) Unknown - pathogenic g.216258040C>G g.216084698C>G - - USH2A_000287 Heterozygous; UV3 PubMed: Aparisi 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/. - c.5167G>C r.(?) p.(Gly1723Arg) - Parent #1 - pathogenic g.216258040C>G g.216084698C>G - - USH2A_000287 - PubMed: Ge 2015 - - Germline - - - - - DNA SEQ-NG - 195-gene panel retinal disease VHM+Y.45 PubMed: Ge 2015 simplex case - - United States - - - - - 1 LOVD
+?/. 25 c.5167G>C r.[4988_5298del,4988_5167del] p.[Glu1663Aspfs*31,Glu1663_Ala1722del] - Unknown ACMG likely pathogenic g.216258040C>G - - - USH2A_000287 mini-gene splicing assay; changes ACMG to likely pathogenic PubMed: Reurink 2022, Journal: Reurink 2022 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.5167G>C r.(?) p.(Gly1723Arg) - Unknown ACMG VUS g.216258040C>G g.216084698C>G - - USH2A_000287 ACMG GN005 criteria: PM2_P PM3_P PP3_P PubMed: Aparisi, M. J. et al., 2014 - rs1342455785 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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