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.

17 entries on 1 page. Showing entries 1 - 17.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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Clinical classification     

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DNA change (hg38)     

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DB-ID     

Variant remarks     

Reference     

ClinVar ID     

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Disease     

ID_report     

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Owner     
+/. - c.14131C>T r.(?) p.(Gln4711Ter) - Unknown - pathogenic g.215844316G>A g.215670974G>A USH2A(NM_206933.2):c.14131C>T (p.Q4711*), USH2A(NM_206933.4):c.14131C>T (p.Q4711*) - USH2A_000400 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.14131C>T r.(?) p.(Gln4711Ter) - Unknown - pathogenic g.215844316G>A g.215670974G>A USH2A(NM_206933.2):c.14131C>T (p.Q4711*), USH2A(NM_206933.4):c.14131C>T (p.Q4711*) - USH2A_000400 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/? 64 c.14131C>T r.(?) p.(Gln4711*) Fibronectin type-III 32 (4633-4730) Unknown - pathogenic g.215844316G>A g.215670974G>A - - USH2A_000400 Heterozygous PubMed: Sandberg 2008 - - Germline - - - - - DNA SEQ - - ? - PubMed: Sandberg 2008 Proband - USH2 or ARRP - - United States - - - - - 1 Anne-Françoise Roux
+/+ 64 c.14131C>T r.(?) p.(Gln4711*) Fibronectin type-III 32 (4633-4730) Unknown - pathogenic g.215844316G>A g.215670974G>A - - USH2A_000400 Heterozygous; mutation PubMed: Krawitz 2014 - - Germline - - - - - DNA SEQ-NG-S - - USH2 - PubMed: Krawitz 2014 Proband F - Germany - - - - - 1 Peter Krawitz
+/+ 64 c.14131C>T r.(?) p.(Gln4711*) Fibronectin type-III 32 (4633-4730) Paternal (inferred) - pathogenic g.215844316G>A g.215670974G>A - - USH2A_000400 Homozygous; mutation PubMed: Krawitz 2014 - - Germline - - - - - DNA SEQ-NG-S - - USH2 - PubMed: Krawitz 2014 Proband F - Germany - - - - - 1 Peter Krawitz
+/+ 64 c.14131C>T r.(?) p.(Gln4711*) Fibronectin type-III 32 (4633-4730) Maternal (inferred) - pathogenic g.215844316G>A g.215670974G>A - - USH2A_000400 Homozygous; mutation PubMed: Krawitz 2014 - - Germline - - - - - DNA SEQ-NG-S - - USH2 - PubMed: Krawitz 2014 Proband F - Germany - - - - - 1 Peter Krawitz
+/+ 64 c.14131C>T r.(?) p.(Gln4711*) Fibronectin type-III 32 (4633-4730) Unknown - pathogenic g.215844316G>A g.215670974G>A - - USH2A_000400 Heterozygous; mutation PubMed: Krawitz 2014 - - Germline - - - - - DNA SEQ-NG-S - - USH2 - PubMed: Krawitz 2014 Proband F - Germany - - - - - 1 Peter Krawitz
+/+ 64 c.14131C>T r.(?) p.(Gln4711*) Fibronectin type-III 32 (4633-4730) Parent #2 - pathogenic g.215844316G>A g.215670974G>A - - USH2A_000400 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - Germany - - - - - 1 Crystel Bonnet
+/+ 64 c.14131C>T r.(?) p.(Gln4711*) Fibronectin type-III 32 (4633-4730) Parent #1 - pathogenic g.215844316G>A g.215670974G>A - - USH2A_000400 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+/. - c.14131C>T r.(?) p.(Gln4711Ter) - Unknown - pathogenic g.215844316G>A g.215670974G>A USH2A(NM_206933.2):c.14131C>T (p.Q4711*), USH2A(NM_206933.4):c.14131C>T (p.Q4711*) - USH2A_000400 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.14131C>T r.(?) p.(Gln4711*) - Parent #2 - likely pathogenic g.215844316G>A g.215670974G>A - - USH2A_000400 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 552 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+/. - c.14131C>T r.(?) p.(Gln4711*) - Parent #2 - pathogenic g.215844316G>A g.215670974G>A - - USH2A_000400 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ - - USH Pat43 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+/. - c.14131C>T r.(?) p.(Gln4711*) - Parent #2 - pathogenic g.215844316G>A g.215670974G>A - - USH2A_000400 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ - - USH Pat42 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
?/. - c.14131C>T r.(?) p.(Gln4711Ter) - Parent #2 - VUS g.215844316G>A g.215670974G>A - - USH2A_000400 - PubMed: Wang 2014 - - Germline - - - - - DNA SEQ-NG - 66-gene panel retinal disease 28 PubMed: Wang 2014 - M - United States - - - - - 1 LOVD
+/. - c.14131C>T r.(?) p.(Gln4711Ter) - Unknown ACMG pathogenic g.215844316G>A - - - USH2A_000400 - PubMed: Mansard et al, 2021 - rs747063294 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.14131C>T r.(?) p.(Gln4711Ter) - Paternal (confirmed) ACMG pathogenic g.215844316G>A - - - USH2A_000400 - PubMed: Mansard et al, 2021 - rs747063294 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+/. - c.14131C>T r.(?) p.(Gln4711Ter) - Unknown ACMG pathogenic g.215844316G>A g.215670974G>A - - USH2A_000400 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Bonnet, C. et al., 2016; PubMed: Mansard, L. et al., 2021; PubMed: Neuhaus, C. et al., 2017 - rs747063294 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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