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.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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Clinical classification     

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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VIP     

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Owner     
+/. - c.12525G>A r.(?) p.(Trp4175*) - Parent #2 - pathogenic g.215848728C>T g.215675386C>T - - USH2A_002008 - PubMed: Neuhaus 2017 - - Germline yes - - - - DNA SEQ - - USH Pat98 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+?/. - c.12525G>A r.(?) p.(Trp4175*) - Parent #1 - likely pathogenic g.215848728C>T g.215675386C>T USH2A, variant 1: c.10712C>T/p.T3571M, variant 2: c.12525G>A/p.W4175* - USH2A_002008 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET4 targeted sequencing panel - see paper retinal disease 248 PubMed: Weisschuh 2020 Filing key number: 84, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+/. - c.12525G>A r.(?) p.(Trp4175Ter) - Unknown ACMG pathogenic g.215848728C>T g.215675386C>T - - USH2A_002008 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Weisschuh, N. et al., 2020; PubMed: Neuhaus, C. et al., 2017 - rs1657987278 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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