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.

9 entries on 1 page. Showing entries 1 - 9.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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Owner     
+/+ 65 c.14225_14232dup r.(?) p.(Val4745Argfs*4) Fibronectin type-III 33 (4732-4825) Paternal (inferred) - pathogenic g.215824045_215824052dup g.215650703_215650710dup - - USH2A_000713 Homozygous PubMed: Baux 2014 - - Germline - - +BccI - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 65 c.14225_14232dup r.(?) p.(Val4745Argfs*4) Fibronectin type-III 33 (4732-4825) Maternal (inferred) - pathogenic g.215824045_215824052dup g.215650703_215650710dup - - USH2A_000713 Homozygous PubMed: Baux 2014 - - Germline - - +BccI - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 65 c.14225_14232dup r.(?) p.(Val4745Argfs*4) Fibronectin type-III 33 (4732-4825) Parent #2 - pathogenic g.215824045_215824052dup g.215650703_215650710dup - - USH2A_000713 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+/. - c.14225_14232dup r.(?) p.(Val4745ArgfsTer4) - Maternal (confirmed) ACMG pathogenic g.215824045_215824052dup - - - USH2A_000713 - PubMed: Mansard et al, 2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.14225_14232dup r.(?) p.(Val4745Argfs*4) - Parent #1 - likely pathogenic g.215824045_215824052dup g.215650703_215650710dup USH2A, variant 1: c.14225_14232dup/p.V4745Rfs*4, variant 2: c.920_923dup/p.H308Qfs*16 - USH2A_000713 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 429 PubMed: Weisschuh 2020 Filing key number: 136, Usher syndrome type 2, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.14225_14232dup r.(?) p.(Val4745Argfs*4) - Parent #1 - likely pathogenic g.215824045_215824052dup g.215650703_215650710dup USH2A, variant 1: c.14225_14232dup/p.V4745Rfs*4, variant 2: c.14225_14232dup/ p.V4745Rfs*4 - USH2A_000713 solved, homozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET5 targeted sequencing panel - see paper retinal disease 622 PubMed: Weisschuh 2020 Filing key number: 222, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.14225_14232dup r.(?) p.(Val4745Argfs*4) - Parent #1 - likely pathogenic g.215824045_215824052dup g.215650703_215650710dup USH2A, variant 1: c.653T>A/p.V218E, variant 2: c.14225_14232dup/ p.V4745Rfs*4 - USH2A_000713 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET4 targeted sequencing panel - see paper retinal disease 603 PubMed: Weisschuh 2020 Filing key number: 217, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.14225_14232dup r.(?) p.(Val4745Argfs*4) - Parent #1 - likely pathogenic g.215824045_215824052dup g.215650703_215650710dup USH2A, variant 1: c.653T>A/p.V218E, variant 2: c.14225_14232dup/ p.V4745Rfs*4 - USH2A_000713 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ blood Sanger sequencing retinal disease 604 PubMed: Weisschuh 2020 Filing key number: 217, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+/. - c.14225_14232dup r.(?) p.(Val4745ArgfsTer4) - Unknown ACMG pathogenic g.215824045_215824052dup g.215650703_215650710dup - - USH2A_000713 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Bonnet, C. et al., 2016; PubMed: Mansard, L. et al., 2021; PubMed: Weisschuh, N. et al., 2020 - rs1657036615 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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