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.

7 entries on 1 page. Showing entries 1 - 7.
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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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Re-site     

VIP     

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Disease     

ID_report     

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Owner     
+?/. - c.6722C>T r.(?) p.(Pro2241Leu) - Unknown - likely pathogenic g.216166445G>A g.215993103G>A - - USH2A_001375 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.6722C>T r.(?) p.(Pro2241Leu) - Unknown - pathogenic g.216166445G>A g.215993103G>A - - USH2A_001375 - PubMed: Haer-Wigman 2017 - - Germline - - - - - DNA SEQ-NG - gene panel ? 5067 PubMed: Haer-Wigman 2017 patient - no Netherlands - - - - - 1 LOVD
+/. - c.6722C>T r.(?) p.(Pro2241Leu) - Parent #2 - pathogenic g.216166445G>A g.215993103G>A - - USH2A_001375 - PubMed: Haer-Wigman 2017 - - Germline - - - - - DNA SEQ-NG - gene panel ? 5866 PubMed: Haer-Wigman 2017 patient - yes Netherlands - - - - - 1 LOVD
+/. - c.6722C>T r.(?) p.(Pro2241Leu) - Parent #1 - pathogenic (recessive) g.216166445G>A g.215993103G>A - - USH2A_001375 - PubMed: Van Huet 2015 - - Germline - - - - - DNA PE, SEQ - APEX retinal disease - PubMed: Van Huet 2015 - - - Netherlands - - - - - 1 LOVD
+?/. 35 c.6722C>T r.(6722c>u) p.(Pro2241Leu) - Parent #1 ACMG likely pathogenic g.216166445G>A g.215993103G>A - - USH2A_001375 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W02-440 Journal: Reurink 2021 - - - Netherlands - - - - - 1 Janine Reurink
+?/. - c.6722C>T r.(?) p.(Pro2241Leu) - Parent #1 ACMG likely pathogenic g.216166445G>A g.215993103G>A USH2A c.6722C>T, p.(Pro2241Leu) - USH2A_001375 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W02-440 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
?/. - c.6722C>T r.(?) p.(Pro2241Leu) - Unknown ACMG VUS g.216166445G>A g.215993103G>A - - USH2A_001375 ACMG GN005 criteria: PM2_P PM3_P PubMed: Reurink, J. et al., 2021 - rs1057518826 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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