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.

14 entries on 1 page. Showing entries 1 - 14.
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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     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

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Consanguinity     

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VIP     

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Panel size     

Owner     
+?/. - c.486-14G>A r.(=) p.(=) - Unknown - likely pathogenic g.216592035C>T g.216418693C>T - - USH2A_000313 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/? 02i c.486-14G>A r.485_486ins486-12_486-1 p.[Met162Ile,Met162_Cys163insCysPheLeuArg] - Parent #1 ACMG likely pathogenic g.216592035C>T g.216418693C>T - - USH2A_000313 Heterozygous; ins last 12 nt IVS2 PubMed: Le Guédard-Méreuze 2010 - rs374536346 Germline - 0/200 controls +BsrI;-MspI;-HpaII;-BsaWI; - - DNA minigene, SEQ - - USH2 - PubMed: Le Guédard-Méreuze 2010 Proband F - France - - - - - 1 Anne-Françoise Roux
+/? 02i c.486-14G>A r.(485_486ins486-12_486-1) p.[(Met162Ile,Met162_Cys163insCysPheLeuArg)] - Paternal (confirmed) ACMG likely pathogenic g.216592035C>T g.216418693C>T - - USH2A_000313 Heterozygous; ins last 12 nt IVS2 (Le Guédard-Méreuze , 2010) PubMed: Baux 2014 - rs374536346 Germline - 0/100 controls +BsrI;-MspI;-HpaII;-BsaWI; - - DNA minigene, SEQ - - USH2 - PubMed: Baux 2014 Proband F - Austria - - - - - 1 Anne-Françoise Roux
+/? 02i c.486-14G>A r.(485_486ins486-12_486-1) p.[(Met162Ile,Met162_Cys163insCysPheLeuArg)] - Paternal (confirmed) ACMG likely pathogenic g.216592035C>T g.216418693C>T - - USH2A_000313 Heterozygous; ins last 12 nt IVS2 (Le Guédard-Méreuze , 2010) PubMed: Baux 2014 - rs374536346 Germline - 0/100 controls +BsrI;-MspI;-HpaII;-BsaWI; - - DNA minigene, SEQ - - USH2 - PubMed: Baux 2014 Relative F - Austria - - - - - 1 Anne-Françoise Roux
+/? 02i c.486-14G>A r.(485_486ins486-12_486-1) p.[(Met162Ile,Met162_Cys163insCysPheLeuArg)] - Maternal (confirmed) ACMG likely pathogenic g.216592035C>T g.216418693C>T - - USH2A_000313 Heterozygous PubMed: Baux 2014 - rs374536346 Germline - 0/200 controls +BsrI;-MspI;-HpaII;-BsaWI; - - DNA arrayCGH, SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/? 02i c.486-14G>A r.(485_486ins486-12_486-1) p.[(Met162Ile,Met162_Cys163insCysPheLeuArg)] - Parent #1 ACMG likely pathogenic g.216592035C>T g.216418693C>T - - USH2A_000313 Heterozygous; Predicted pathogenic PubMed: Neveling 2012 - rs374536346 Germline - - +BsrI;-MspI;-HpaII;-BsaWI; - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Neveling 2012 Proband M - - - - - - - 1 Anne-Françoise Roux
+/? 02i c.486-14G>A r.(485_486ins486-12_486-1) p.[(Met162Ile,Met162_Cys163insCysPheLeuArg)] - Parent #1 ACMG likely pathogenic g.216592035C>T g.216418693C>T - - USH2A_000313 Heterozygous; Predicted pathogenic PubMed: Neveling 2012 - rs374536346 Germline - - +BsrI;-MspI;-HpaII;-BsaWI; - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Neveling 2012 Proband M - - - - - - - 1 Anne-Françoise Roux
+/? 02i c.486-14G>A r.485_486ins486-12_486-1 p.[Met162Ile,Met162_Cys163insCysPheLeuArg] - Unknown ACMG likely pathogenic g.216592035C>T g.216418693C>T - - USH2A_000313 Heterozygous; ins last 12 nt IVS2 PubMed: Zhao 2014 - rs374536346 Germline - 0/200 controls +BsrI;-MspI;-HpaII;-BsaWI; - - DNA SEQ - - RPar - PubMed: Zhao 2014 Proband - - Japan - - - - - 1 Anne-Françoise Roux
+/. - c.486-14G>A r.spl? p.? - Unknown - pathogenic g.216592035C>T g.216418693C>T - - USH2A_000313 - PubMed: Haer-Wigman 2017 - - Germline - - - - - DNA SEQ-NG - gene panel ? 3808 PubMed: Haer-Wigman 2017 patient - no Netherlands - - - - - 1 LOVD
+/. 2i c.486-14G>A r.spl p.? - Parent #2 - pathogenic (recessive) g.216592035C>T g.216418693C>T - - USH2A_000313 - PubMed: Dad 2016 - - Germline - - - - - DNA SEQ-NG - gene panel USH retinal disease USH2-9 PubMed: Dad 2016 - M no Denmark - - - - - 1 LOVD
+/. - c.486-14G>A r.spl p.? - Parent #1 - pathogenic g.216592035C>T g.216418693C>T - - USH2A_000313 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ - - USH Pat15 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+?/. - c.486-14G>A r.(=) p.(=) - Unknown ACMG VUS g.216592035C>T - - - USH2A_000313 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - USH IR_GH_0031 - - M - Korea, South (Republic) - - - - - 1 Jinu Han
+/. - c.486-14G>A r.spl p.? - Both (homozygous) ACMG pathogenic g.216592035C>T g.216418693C>T - - USH2A_000313 - Villafuerte-de la Cruz RA, et al., 2023. Submitted ClinVar-372543 rs374536346 Germline yes - - - - DNA SEQ-NG-I Buccal swab - USH2A 2487313 Villafuerte-de la Cruz RA, et al., 2023. Submitted - M likely Mexico Hispanic - - - None 1 Rocio Villafuerte-de la Cruz
?/. - c.486-14G>A r.spl p.? - Unknown ACMG VUS g.216592035C>T g.216418693C>T - - USH2A_000313 ACMG GN005 criteria: PM2_P PM3_P PubMed: Neuhaus, C. et al., 2017 - rs374536346 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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