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.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

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AscendingDNA change (cDNA)     

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DNA change (hg38)     

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+/. - c.12394del r.(?) p.(Leu4132Trpfs*35) - Parent #1 - pathogenic g.215848859del - [12394del;14074G>A] - USH2A_001328 - PubMed: Haer-Wigman 2017 - - Germline - - - - - DNA SEQ-NG - gene panel ? 1977 PubMed: Haer-Wigman 2017 patient - no Netherlands - - - - - 1 LOVD
+/. 63 c.12394del r.(?) p.(Leu4132Trpfs*35) - Both (homozygous) ACMG pathogenic (recessive) g.215848859del - - - USH2A_001328 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH2A Pat23 PubMed: Bahena 2021 - F yes Iran - - - - - 2 Barbara Vona
+?/. - c.12394del r.(?) p.(Leu4132Trpfs*35) - Parent #1 - likely pathogenic g.215848861del g.215675519del USH2A, variant 1: c.12394del/p.L4132Wfs*35, variant 2: c.12394del/p.L4132Wfs*35 - USH2A_001328 solved, homozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET6 targeted sequencing panel - see paper retinal disease 677 PubMed: Weisschuh 2020 Filing key number: 245, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+/. - c.12394del r.(?) p.(Leu4132TrpfsTer35) - Unknown ACMG pathogenic g.215848861del g.215675519del 12394delC - USH2A_001328 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Bahena, P. et al., 2022 - rs1558049084 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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