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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Effect     

Exon     

AscendingDNA change (cDNA)     

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+/+ 26 c.5278del r.(?) p.(Asp1760Metfs*10) Laminin G-like 2 (1714-1891) Parent #1 - pathogenic g.216256818del g.216083476del 5278delG - USH2A_000672 Heterozygous; Pathogenic PubMed: Jaijo 2010 - - Germline - - -BccI - - DNA SEQ, SSCA - - USH2 - PubMed: Jaijo 2010 Proband M - Spain - - - - - 1 Jose Maria Millan
+/+ 26 c.5278del r.(?) p.(Asp1760Metfs*10) Laminin G-like 2 (1714-1891) Paternal (inferred) - pathogenic g.216256818del g.216083476del 5278delG - USH2A_000672 Homozygous PubMed: Aparisi 2014 - - Germline - - -BccI - - DNA SEQ, SEQ-NG-S - - USH3 - PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/+ 26 c.5278del r.(?) p.(Asp1760Metfs*10) Laminin G-like 2 (1714-1891) Maternal (inferred) - pathogenic g.216256818del g.216083476del 5278delG - USH2A_000672 Homozygous PubMed: Aparisi 2014 - - Germline - - -BccI - - DNA SEQ, SEQ-NG-S - - USH3 - PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+?/. - c.5278del r.(?) p.(Asp1760Metfs*10) - Unknown - likely pathogenic g.216256818del g.216083476del NM_206933, c.5278del, p.Asp1760MetfsTer10 - USH2A_000672 - PubMed: Ezquerra-Inchausti 2018 - - Germline yes - - - - DNA SEQ-NG blood - retinal disease II:1 PubMed: Ezquerra-Inchausti 2018 Family RP34, II:1 ? no Spain - - - - - 1 LOVD
+?/. - c.5278del r.(?) p.(Asp1760Metfs*10) - Unknown - likely pathogenic g.216256818del g.216083476del c.5278del, p.Asp1760MetfsTer10 - USH2A_000672 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI2893_004478 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+/. - c.5278del r.(?) p.(Asp1760Metfs*10) - Unknown ACMG pathogenic g.216256818del g.216083476del - - USH2A_000672 - Villafuerte-de la Cruz RA, et al., 2023. Submitted ClinVar-555362 rs754374132 Germline yes - - - - DNA SEQ-NG-I - - USH2A 2694923 Villafuerte-de la Cruz RA, et al., 2023. Submitted - F likely Mexico Hispanic - - - NONE 1 Rocio Villafuerte-de la Cruz
+/. - c.5278del r.(?) p.(Asp1760MetfsTer10) - Unknown ACMG pathogenic g.216256818del g.216083476del 5278delG - USH2A_000672 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Garcia-Garcia, G. et al., 2011; PubMed: Aparisi, M. J. et al., 2014; PubMed: Sloan-Heggen, C. M. et al., 2016 - rs754374132 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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