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.

8 entries on 1 page. Showing entries 1 - 8.
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AscendingDNA change (cDNA)     

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+/+ 41 c.7950dup r.(?) p.(Asn2651Glnfs*10) Fibronectin type-III 13 (2621-2718) Parent #2 - pathogenic g.216062044dup g.215888702dup 7950dupC - USH2A_001014 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+/. - c.7950dup r.(?) p.(Asn2651GlnfsTer10) - Unknown - pathogenic g.216062044dup g.215888702dup USH2A(NM_206933.2):c.7950dup (p.(Asn2651GlnfsTer10)), USH2A(NM_206933.4):c.7950dupC (p.N2651Qfs*10) - USH2A_001014 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.7950dup r.(?) p.(Asn2651Glnfs*10) - Unknown - pathogenic g.216062044dup g.215888702dup - - USH2A_001014 - PubMed: Haer-Wigman 2017 - - Germline - - - - - DNA SEQ-NG - gene panel ? 720 PubMed: Haer-Wigman 2017 patient - no Netherlands - - - - - 1 LOVD
+?/. - c.7950dup r.(?) p.(Asn2651Glnfs*10) - Parent #1 - likely pathogenic g.216062044dup g.215888702dup USH2A, variant 1: c.7950dup/p.N2651Qfs*10, variant 2: c.11864G>A/p.W3955* - USH2A_001014 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET5 targeted sequencing panel - see paper retinal disease 642 PubMed: Weisschuh 2020 Filing key number: 229, Usher syndrome type 2, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.7950dup r.(?) p.(Asn2651Glnfs*10) - Parent #1 - likely pathogenic g.216062044dup g.215888702dup USH2A, variant 1: c.7950dup/p.N2651Qfs*10, variant 2: c.15063_15081delinsGC/ p.T5022Qfs*150 - USH2A_001014 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET5 targeted sequencing panel - see paper retinal disease 658 PubMed: Weisschuh 2020 Filing key number: 235, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.7950dup r.(?) p.(Asn2651Glnfs*10) - Parent #1 - likely pathogenic g.216062044dup g.215888702dup USH2A, variant 1: c.7950dup/p.N2651Qfs*10, variant 2: c.2299del/p.E767Sfs*21 - USH2A_001014 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 774 PubMed: Weisschuh 2020 Filing key number: 300, Usher syndrome type 2, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. - c.7950dup r.(?) p.(Asn2651GlnfsTer10) - Unknown - pathogenic g.216062044dup - USH2A(NM_206933.2):c.7950dup (p.(Asn2651GlnfsTer10)), USH2A(NM_206933.4):c.7950dupC (p.N2651Qfs*10) - USH2A_001014 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.7950dup r.(?) p.(Asn2651GlnfsTer10) - Unknown ACMG pathogenic g.216062044dup g.215888702dup 7950dupC - USH2A_001014 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Bonnet, C. et al., 2016; PubMed: Weisschuh, N. et al., 2020 - rs886041502 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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