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.

16 entries on 1 page. Showing entries 1 - 16.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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Owner     
+/? 33i c.6485+5G>A r.6326_6485del p.Asp2109Glyfs*7 Fibronectin type-III 7 (2052-2138) Parent #1 ACMG likely pathogenic g.216173740C>T g.216000398C>T - - USH2A_000146 Heterozygous; E33 skipping (Nakanishi , 2010) PubMed: Nakanishi 2009 - - Germline - 0/270 controls - - - DNA, RNA RT-PCR, SEQ - - USH2 - PubMed: Nakanishi 2009 Proband F - Japan - - - - - 1 Anne-Françoise Roux
+?/. - c.6485+5G>A r.spl p.? - Parent #1 - likely pathogenic g.216173740C>T g.216000398C>T - - USH2A_000146 - PubMed: Huang 2018 - - Germline - - - - - DNA SEQ-NG - 283-gene panel retinal disease RP046 PubMed: Huang 2018 - - - - - - - - - 1 LOVD
+/. 33i c.6485+5G>A r.spl? p.(?) - Paternal (confirmed) - pathogenic g.216173740C>T g.216000398C>T c.6485+5G>A - USH2A_000146 - PubMed: Fu 2018 - - Germline yes - - - - DNA SEQ-NG-I, SEQ blood Whole-exome sequencing retinal disease D-II-2 PubMed: Fu 2018 - M no China - - - - - 1 LOVD
+/. 33i c.6485+5G>A r.spl? p.(?) - Paternal (confirmed) - pathogenic g.216173740C>T g.216000398C>T c.6485+5G>A - USH2A_000146 - PubMed: Fu 2018 - - Germline yes - - - - DNA SEQ-NG-I, SEQ blood Whole-exome sequencing retinal disease D-II-2 PubMed: Fu 2018 - F no China - - - - - 1 LOVD
+?/. 33i c.6485+5G>A r.spl? p.? - Unknown - likely pathogenic (recessive) g.216173740C>T - c.6485+5G>A - USH2A_000146 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - F - - - - - - - 1 LOVD
+?/. 33i c.6485+5G>A r.spl? p.(?) - Parent #1 ACMG likely pathogenic g.216173740C>T g.216000398C>T USH2A c.6485+5G>A, - - USH2A_000146 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes retinal disease 61 PubMed: Meng 2020 - F - China - - - - - 1 LOVD
+?/. 33i c.6485+5G>A r.spl? p.(?) - Parent #2 ACMG likely pathogenic g.216173740C>T g.216000398C>T USH2A c.6485+5G>A, - - USH2A_000146 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes retinal disease 56 PubMed: Meng 2020 - M - China - - - - - 1 LOVD
+/. - c.6485+5G>A r.spl? p.(?) - Parent #1 - pathogenic g.216173740C>T g.216000398C>T USH2A c.6485+5G>A, - - USH2A_000146 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD190332A PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+/. - c.6485+5G>A r.spl p.(?) - Parent #1 - pathogenic g.216173740C>T g.216000398C>T USH2A c.6485+5G>A, - - USH2A_000146 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH DTP1900305 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+/. 33i c.6485+5G>A r.spl p.(Asp2109Glyfs*7) - Parent #1 ACMG pathogenic g.216173740C>T g.216000398C>T USH2A c.6485+5G>A, p.Asp2109Glyfs*7 - USH2A_000146 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 41554658 PubMed: Zhu 2021 family 166, patient 41554658 F - China - - - - - 1 LOVD
+/. 33i c.6485+5G>A r.spl p.(Asp2109Glyfs*7) - Parent #1 ACMG pathogenic g.216173740C>T g.216000398C>T USH2A c.6485+5G>A, p.Asp2109Glyfs*7 - USH2A_000146 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 43028663 PubMed: Zhu 2021 family 57, patient 43028663 F - China - - - - - 1 LOVD
+/. 33i c.6485+5G>A r.spl p.(Asp2109Glyfs*7) - Parent #1 ACMG pathogenic g.216173740C>T g.216000398C>T USH2A c.6485+5G>A, p.Asp2109Glyfs*7 - USH2A_000146 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF_1998 PubMed: Zhu 2021 family 171, patient SRF_1998 M - China - - - - - 1 LOVD
+/. 33i c.6485+5G>A r.spl p.(Asp2109Glyfs*7) - Parent #1 ACMG pathogenic g.216173740C>T g.216000398C>T USH2A c.6485+5G>A, p.Asp2109Glyfs*7 - USH2A_000146 with two variants in MYO7A gene PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 43868772 PubMed: Zhu 2021 family 225, patient 43868772 M - China - - - - - 1 LOVD
+/. 33i c.6485+5G>A r.spl p.(Asp2109Glyfs*7) - Parent #1 ACMG pathogenic g.216173740C>T g.216000398C>T USH2A c.6485+5G>A, p.Asp2109Glyfs*7 - USH2A_000146 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 41554659 PubMed: Zhu 2021 family 166, patient 41554659 M - China - - - - - 1 LOVD
+/. 33i c.6485+5G>A r.spl p.(Asp2109Glyfs*7) - Parent #2 ACMG pathogenic g.216173740C>T g.216000398C>T USH2A c.6485+5G>A, p.Asp2109Glyfs*7 - USH2A_000146 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 43637867 PubMed: Zhu 2021 family 14, patient 43637867 M - China - - - - - 1 LOVD
+?/. - c.6485+5G>A r.spl p.? - Unknown ACMG likely pathogenic g.216173740C>T g.216000398C>T - - USH2A_000146 ACMG GN005 criteria: PM2_P PM3_S PP1_P PP3_P PubMed: Gao, F. J. et al., 2021; PubMed: Meng, X. et al., 2021; PubMed: Fu, Y. C. et al., 2018 - rs1668240410 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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