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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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+/. - c.4517_4518del r.(?) p.(Glu1506Valfs*23) - Parent #1 - pathogenic g.216348708_216348709del g.216175366_216175367del USH2A c.4517_4518delCT, p.Arg1505Serfs*7 - USH2A_002575 error in annotation, deleted nucleotides probably written from genomic (reverse) variant; should be AG instead of CT; (rs866243264); protein annotation should be p.(Glu1506Valfs*23); heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH DT19001018 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+/. 21 c.4517_4518del r.(?) p.(Glu1506Valfs*23) - Parent #1 ACMG pathogenic g.216348708_216348709del g.216175366_216175367del USH2A c.4517_4518delCT - USH2A_002575 Variant reference (CT) does not agree with reference sequence (AG), probably a reverse complement error (from genomic annotation); should be c.4517_4518delAG; no protein annotation written PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease AXLM_29 PubMed: Zhu 2021 family 147, patient AXLM_29 F - China - - - - - 1 LOVD
+/. 21 c.4517_4518del r.(?) p.(Glu1506Valfs*23) - Parent #1 ACMG pathogenic g.216348708_216348709del g.216175366_216175367del USH2A c.4517_4518delCT - USH2A_002575 Variant reference (CT) does not agree with reference sequence (AG), probably a reverse complement error (from genomic annotation); should be c.4517_4518delAG; no protein annotation written PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease AXLM_28 PubMed: Zhu 2021 family 147, patient AXLM_28 F - China - - - - - 1 LOVD
+/. - c.4517_4518del r.(?) p.(Glu1506ValfsTer23) - Unknown ACMG pathogenic g.216348708_216348709del g.216175366_216175367del 4517_4518delAG - USH2A_002575 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Gao, F. J. et al., 2021; PubMed: Meng, X. et al., 2021 - rs866243264 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
?/. 21 c.4517_4518delAG r.(?) p.(Glu1506Valfs*23) - Parent #1 ACMG VUS g.216348708_216348709del g.216175366_216175367del USH2A c.4517_4518delAG, p.Glu1506Valfs*23 - USH2A_002575 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes USH 18 PubMed: Meng 2020 - F - China - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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