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     

Protein     

P-domain     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

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Disease     

ID_report     

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Owner     
+/. - c.6741del r.(?) p.(Ala2249Profs*30) - Parent #1 ACMG pathogenic (recessive) g.216166430del g.215993088del c.6741delC - USH2A_001860 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19658 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+/. - c.6741del r.(?) p.(Ala2249Profs*30) - Parent #1 ACMG pathogenic (recessive) g.216166430del g.215993088del c.6741delC - USH2A_001860 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ - - HL 19893 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+/. - c.6741del r.(?) p.(Ala2249Profs*30) - Parent #1 ACMG pathogenic (recessive) g.216166430del g.215993088del c.6741delC - USH2A_001860 - PubMed: Sun 2018 - - Germline - - - - - DNA MLPA, SEQ-NG - - HL 19708 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+/. - c.6741del r.(?) p.(Ala2249Profs*30) - Parent #2 ACMG pathogenic (recessive) g.216166430del g.215993088del c.6741delC - USH2A_001860 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19658 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+/. - c.6741del r.(?) p.(Ala2249Profs*30) - Parent #2 - pathogenic g.216166430del g.215993088del USH2A c.6741delC, p.Ala2249ProfsTer30 - USH2A_001860 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH DP18085405 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+/. - c.6741del r.(?) p.(Ala2249ProfsTer30) - Unknown ACMG pathogenic g.216166430del g.215993088del 6741delC - USH2A_001860 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Gao, F. J. et al., 2021; PubMed: Sun, T. et al., 2018; PubMed: Meng, X. et al., 2021 - rs1335175914 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+?/. 35 c.6741delC r.(?) p.(Ala2249Profs*30) - Parent #2 ACMG likely pathogenic g.216166430del g.215993088del USH2A c.6741delC, p.Ala2249Profs*30 - USH2A_001860 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes USH 29 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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