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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?/. - c.7915T>C r.(?) p.(Ser2639Pro) - Unknown - VUS g.216062076A>G g.215888734A>G USH2A(NM_206933.2):c.7915T>C (p.S2639P) - USH2A_000422 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/? 41 c.7915T>C r.(?) p.(Ser2639Pro) Fibronectin type-III 13 (2621-2718) Unknown ACMG VUS g.216062076A>G g.215888734A>G - - USH2A_000422 Heterozygous; benign PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 2 Anne-Françoise Roux
?/? 41 c.7915T>C r.(?) p.(Ser2639Pro) Fibronectin type-III 13 (2621-2718) Unknown ACMG VUS g.216062076A>G g.215888734A>G - - USH2A_000422 Heterozygous; UV2 PubMed: Garcia-Garcia 2011, USMA missense analysis, missense variant in MSV3d - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2011 Proband M - Spain - - - - - 1 Jose Maria Millan
?/? 41 c.7915T>C r.(?) p.(Ser2639Pro) Fibronectin type-III 13 (2621-2718) Paternal (inferred) ACMG VUS g.216062076A>G g.215888734A>G - - USH2A_000422 Homozygous; likely deleterious PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - Italy - - - - - 1 Crystel Bonnet
?/? 41 c.7915T>C r.(?) p.(Ser2639Pro) Fibronectin type-III 13 (2621-2718) Maternal (inferred) ACMG VUS g.216062076A>G g.215888734A>G - - USH2A_000422 Homozygous; likely deleterious PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - Italy - - - - - 1 Crystel Bonnet
+?/. 41 c.7915T>C r.(?) p.(Ser2639Pro) - Parent #2 ACMG likely pathogenic (recessive) g.216062076A>G - - - USH2A_000422 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH Pat29 PubMed: Bahena 2021 - F no Iran - - - - - 3 Barbara Vona
+?/. 41 c.7915T>C r.(?) p.(Ser2639Pro) - Unknown - likely pathogenic (recessive) g.216062076A>G - c.7915T>C - USH2A_000422 - PubMed: Colombo-2020 - rs398124620 Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
+?/. 41 c.7915T>C r.(?) p.(Ser2639Pro) - Unknown - likely pathogenic (recessive) g.216062076A>G - c.7915T>C - USH2A_000422 - PubMed: Colombo-2020 - rs398124620 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+?/+? 41 c.7915T>C r.(?) p.(Ser2639Pro) - Unknown ACMG likely pathogenic g.216062076A>G g.215888734A>G - - USH2A_000422 PM2_Sup, PM3_St, PP1_M, PP3 - ClinVar-96667 rs398124620 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.7915T>C r.(?) p.(Ser2639Pro) - Unknown ACMG VUS g.216062076A>G g.215888734A>G - - USH2A_000422 ACMG GN005 criteria: PM2_P PM3_M PubMed: Bonnet, C. et al., 2016; PubMed: Colombo, L. et al., 2022; PubMed: Bahena, P. et al., 2022; PubMed: Colombo, L. et al., 2021 - rs398124620 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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