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.

22 entries on 1 page. Showing entries 1 - 22.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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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     

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Disease     

ID_report     

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Owner     
+/+ 24 c.4957C>T r.(?) p.(Arg1653*) Laminin G-like 1 (1517-1709) Maternal (confirmed) - pathogenic g.216260091G>A g.216086749G>A - - USH2A_000288 Heterozygous PubMed: Baux 2014 - - Germline - - -BstUI;-FauI;-AciI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Relative M - France - - - - - 1 Anne-Françoise Roux
+/+ 24 c.4957C>T r.(?) p.(Arg1653*) Laminin G-like 1 (1517-1709) Maternal (confirmed) - pathogenic g.216260091G>A g.216086749G>A - - USH2A_000288 Heterozygous PubMed: Baux 2014 - - Germline - - -BstUI;-FauI;-AciI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 24 c.4957C>T r.(?) p.(Arg1653*) Laminin G-like 1 (1517-1709) Paternal (inferred) - pathogenic g.216260091G>A g.216086749G>A - - USH2A_000288 Heterozygous PubMed: Baux 2014 - - Germline - - -BstUI;-FauI;-AciI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 24 c.4957C>T r.(?) p.(Arg1653*) Laminin G-like 1 (1517-1709) Parent #1 - pathogenic g.216260091G>A g.216086749G>A - - USH2A_000288 Heterozygous PubMed: Baux 2014 - - Germline - - -BstUI;-FauI;-AciI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Relative M - France - - - - - 1 Anne-Françoise Roux
+/+ 24 c.4957C>T r.(?) p.(Arg1653*) Laminin G-like 1 (1517-1709) Parent #1 - pathogenic g.216260091G>A g.216086749G>A - - USH2A_000288 Heterozygous; Pathogenic PubMed: Neveling 2012 - - Germline - - -BstUI;-FauI;-AciI; - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Neveling 2012 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 24 c.4957C>T r.(?) p.(Arg1653*) Laminin G-like 1 (1517-1709) Parent #1 - pathogenic g.216260091G>A g.216086749G>A - - USH2A_000288 Heterozygous; mutation PubMed: Bonnet 2016 - rs754768875 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/. 24 c.4957C>T r.(?) p.(Arg1653*) Laminin G-like 1 (1517-1709) Parent #2 - pathogenic (recessive) g.216260091G>A - - - USH2A_000288 - PubMed: Ivanova 2018 - - Germline - - -BstUI;-FauI;-AciI; - - DNA SEQ-NG-S - - USH2 Pat5 PubMed: Ivanova 2018 Proband M - Russian Federation Slavonian;Ukraine - - - - 1 Vladimir Strelnikov
+/. 24 c.4957C>T r.(?) p.(Arg1653*) Laminin G-like 1 (1517-1709) Parent #2 - pathogenic (recessive) g.216260091G>A - - - USH2A_000288 - PubMed: Ivanova 2018 - - Germline - - -BstUI;-FauI;-AciI; - - DNA SEQ-NG-S - - USH2 Pat9 PubMed: Ivanova 2018 - F - Russian Federation Slavonian - - - - 1 Vladimir Strelnikov
+?/. - c.4957C>T r.(?) p.(Arg1653*) - Parent #1 - likely pathogenic g.216260091G>A g.216086749G>A - - USH2A_000288 - PubMed: Huang 2017 - - Germline - - - - - DNA SEQ-NG - WES retinal disease RP-063 PubMed: Huang 2017 patient - - China - - - - - 1 LOVD
+/. 24 c.4957C>T r.(?) p.(Arg1653*) - Parent #2 - pathogenic (recessive) g.216260091G>A g.216086749G>A - - USH2A_000288 possible duplicate PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-45 (D42) PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - F no Denmark - - - - - 1 Anne-Françoise Roux
+?/. - c.4957C>T r.(?) p.(Arg1653*) - Unknown ACMG pathogenic g.216260091G>A - - - USH2A_000288 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - RP IR_SS_0016 - - F - Korea, South (Republic) - - - - - 1 Jinu Han
+/. 24 c.4957C>T r.(?) p.(Arg1653*) - Unknown ACMG pathogenic g.216260091G>A g.216086749G>A NM_206933.2:c.4957C>T, NP_996816.2:p.(Arg1653Ter), NC_000001.10:g.216260091G>A - USH2A_000288 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - exome sequencing retinal disease 2016101712 PubMed: Wang 2018 - F ? China Han Chinese - - - - 1 LOVD
+?/. - c.4957C>T r.(?) p.(Arg1653*) - Unknown ACMG likely pathogenic g.216260091G>A g.216086749G>A USH2A c.4957C>T, p.(Arg1653*), c.5074G>T, p.(Asp1692Tyr) - USH2A_000288 - PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 288 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
+?/. - c.4957C>T r.(?) p.(Arg1653*) - Unknown ACMG likely pathogenic g.216260091G>A g.216086749G>A USH2A c.4957C>T, p.(Arg1653*) - USH2A_000288 single heterozygous variant (recessive) PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 485 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
+/. - c.4957C>T r.(?) p.(Arg1653Ter) - Unknown ACMG pathogenic g.216260091G>A g.216086749G>A USH2A c.C4957T, p.R1653X - USH2A_000288 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 114 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
+?/. 24 c.4957C>T r.(?) p.(Arg1653*) - Unknown - likely pathogenic (recessive) g.216260091G>A - c.4957C>T - USH2A_000288 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - WES retinal disease - PubMed: Liu-2020 - F - - - - - - - 1 LOVD
+/. 24 c.4957C>T r.(?) p.(Arg1653*) - Unknown - pathogenic (recessive) g.216260091G>A - c.4957C>T - USH2A_000288 - PubMed: Colombo-2020 - rs754768875 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
+?/. 24 c.4957C>T r.(?) p.(Arg1653*) - Parent #1 ACMG likely pathogenic g.216260091G>A g.216086749G>A USH2A c.4957C>T, p.Arg1653* - USH2A_000288 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes retinal disease 55 PubMed: Meng 2020 - M - China - - - - - 1 LOVD
+/. 24 c.4957C>T r.(?) p.(Arg1653*) - Parent #1 ACMG pathogenic g.216260091G>A g.216086749G>A USH2A c.4957C>T, p.R1653* - USH2A_000288 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease AXLM_25 PubMed: Zhu 2021 family 109, patient AXLM_25 M - China - - - - - 1 LOVD
+/. 24 c.4957C>T r.(?) p.(Arg1653*) - Parent #2 ACMG pathogenic g.216260091G>A g.216086749G>A USH2A c.4957C>T, p.R1653* - USH2A_000288 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease HSR575 PubMed: Zhu 2021 family 86, patient HSR575 M - China - - - - - 1 LOVD
+/. - c.4957C>T r.(?) p.(Arg1653*) - Unknown - pathogenic g.216260091G>A - - - USH2A_000288 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.4957C>T r.(?) p.(Arg1653Ter) - Unknown ACMG likely pathogenic g.216260091G>A g.216086749G>A - - USH2A_000288 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Ma, D. J. et al., 2021; PubMed: Meng, X. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Colombo, L. et al., 2021 - rs754768875 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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