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)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

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Disease     

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Owner     
+?/. - c.8917_8918del r.(?) p.(Leu2973LysfsTer79) - Parent #2 - likely pathogenic g.216019307_216019308del g.215845965_215845966del 8917_8918delCT - USH2A_002084 - - - - Germline yes - - - - DNA SEQ-NG - 284 gene panel retinal disease W272-1 PubMed: Huang 2015 - M - China - - - - - 1 LOVD
+/. 45 c.8917_8918del r.(?) p.(Leu2973Lysfs*79) - Parent #2 ACMG pathogenic g.216019307_216019308del g.215845965_215845966del USH2A c.8917_8918delCT - USH2A_002084 no protein annotation written PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease W272-1 PubMed: Zhu 2021 family 241, patient W272-1 M - China - - - - - 1 LOVD
+/. - c.8917_8918del r.(?) p.(Leu2973LysfsTer79) - Unknown ACMG pathogenic g.216019307_216019308del g.215845965_215845966del 8917_8918delCT - USH2A_002084 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Wafa, T. T. et al., 2021; PubMed: Mansard, L. et al., 2021; PubMed: Huang, X. F. et al., 2015 - rs1553268582 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.8917_8918del r.(?) p.(Leu2973LysfsTer79) - Unknown ACMG pathogenic (recessive) g.216019307_216019308del g.215845965_215845966del - - USH2A_002084 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? SRP-1240 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - 1 Johan den Dunnen
+/. - c.8917_8918delCT r.(?) p.(Leu2973LysfsTer79) - Unknown ACMG pathogenic g.216019307_216019308del - - - USH2A_002084 - PubMed: Mansard et al, 2021 - rs1553268582 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+/. - c.8917_8918delCT r.(?) p.(Leu2973Lysfs*79) - Unknown ACMG pathogenic g.216019307_216019308del g.215845965_215845966del USH2A c.8917_8918delCT, p.(Leu2973Lysfs*79) - USH2A_002084 heterozygous PubMed: Dineiro 2020 - - Germline ? - - - - DNA SEQ-NG-I, SEQ blood, saliva targeted sequencing with 1 of 4 panels of OFTALMOgenics probes retinal disease OFTALMO.077 PubMed: Dineiro 2020 - ? - Spain - - - - - 1 LOVD
+?/. 45 c.8917_8918delCT r.(?) p.(Leu2973Lysfs*79) - Both (homozygous) - likely pathogenic g.216019303_216019304delAG - c.8917-8198delCT, p.L2973Kfs*79 - USH2A_002084 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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