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.

11 entries on 1 page. Showing entries 1 - 11.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

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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Re-site     

VIP     

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Template     

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Disease     

ID_report     

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Panel size     

Owner     
+?/? 69 c.15017C>T r.(?) p.(Thr5006Met) Fibronectin type-III 35 (4928-5014) Parent #1 ACMG VUS g.215812532G>A g.215639190G>A - - USH2A_001053 Heterozygous; mutation PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - rs757676723 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Denmark - - - - - 1 Crystel Bonnet
+?/? 69 c.15017C>T r.(?) p.(Thr5006Met) Fibronectin type-III 35 (4928-5014) Parent #2 ACMG VUS g.215812532G>A g.215639190G>A - - USH2A_001053 Heterozygous; mutation PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - rs757676723 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/? 69 c.15017C>T r.(?) p.(Thr5006Met) Fibronectin type-III 35 (4928-5014) Paternal (inferred) ACMG VUS g.215812532G>A g.215639190G>A - - USH2A_001053 Homozygous; mutation {PMID27460420:Bonnet et al., 2016}, USMA missense analysis, missense variant in MSV3d - rs757676723 Germline - - - - - DNA SEQ - - USH2 - PubMed: Abdi 2016 Proband F - Algeria - - - - - 1 Crystel Bonnet
+?/? 69 c.15017C>T r.(?) p.(Thr5006Met) Fibronectin type-III 35 (4928-5014) Maternal (inferred) ACMG VUS g.215812532G>A g.215639190G>A - - USH2A_001053 Homozygous; mutation {PMID27460420:Bonnet et al., 2016}, USMA missense analysis, missense variant in MSV3d - rs757676723 Germline - - - - - DNA SEQ - - USH2 - PubMed: Abdi 2016 Proband F - Algeria - - - - - 1 Crystel Bonnet
+/. - c.15017C>T r.(?) p.(Thr5006Met) - Both (homozygous) - pathogenic g.215812532G>A g.215639190G>A - - USH2A_001053 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ-NG - gene panel USH Pat91 PubMed: Neuhaus 2017 - - yes Saudi Arabia - - - - - 1 LOVD
+?/. - c.15017C>T r.(?) p.(Thr5006Met) - Parent #1 - likely pathogenic g.215812532G>A g.215639190G>A - - USH2A_001053 - PubMed: Huang 2015 - - Germline yes - - - - DNA SEQ-NG - 284 gene panel retinal disease H12-1 PubMed: Huang 2015 - F - China - - - - - 1 LOVD
+?/. - c.15017C>T r.(?) p.(Thr5006Met) - Unknown - likely pathogenic g.215812532G>A g.215639190G>A USH2A c.15017C>T, p.Thr5006Met - USH2A_001053 Conflicting in silico model predictions, heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI2943_004528 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. 69 c.15017C>T r.(?) p.(Thr5006Met) - Unknown - likely pathogenic g.215812532G>A - c.15017C>T,p.T5006M - USH2A_001053 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+/. - c.15017C>T r.(?) p.(Thr5006Met) - Parent #1 - pathogenic g.215812532G>A g.215639190G>A USH2A c.15017C>T, p.Thr5006Met - USH2A_001053 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD190332 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+/. - c.15017C>T r.(?) p.(Thr5006Met) - Parent #1 - pathogenic g.215812532G>A g.215639190G>A USH2A c.15017C>T, p.Thr5006Met - USH2A_001053 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD190400A PubMed: Gao 2021 - F - China - - - - - 1 LOVD
?/. - c.15017C>T r.(?) p.(Thr5006Met) - Unknown ACMG VUS g.215812532G>C g.215639190G>C - - USH2A_001053 ACMG GN005 criteria: PM2_P PM3_S PubMed: Gao, F. J. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Huang, X. F. et al., 2015; PubMed: Neuhaus, C. et al., 2017 - rs757676723 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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