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.

21 entries on 1 page. Showing entries 1 - 21.
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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)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

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Disease     

ID_report     

Reference     

Remarks     

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Consanguinity     

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VIP     

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Panel size     

Owner     
+/. - c.1227G>A r.(?) p.(Trp409Ter) - Unknown - pathogenic g.216497611C>T g.216324269C>T USH2A(NM_206933.2):c.1227G>A (p.W409*), USH2A(NM_206933.4):c.1227G>A (p.W409*) - USH2A_000156 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1227G>A r.(?) p.(Trp409Ter) - Unknown - pathogenic g.216497611C>T g.216324269C>T USH2A(NM_206933.2):c.1227G>A (p.W409*), USH2A(NM_206933.4):c.1227G>A (p.W409*) - USH2A_000156 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 7 c.1227G>A r.(?) p.(Trp409*) Laminin N-terminal (271-517) Paternal (inferred) - pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 Homozygous PubMed: Pennings 2004 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Pennings 2004 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1227G>A r.(?) p.(Trp409*) Laminin N-terminal (271-517) Maternal (inferred) - pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 Homozygous PubMed: Pennings 2004 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Pennings 2004 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1227G>A r.(?) p.(Trp409*) Laminin N-terminal (271-517) Paternal (inferred) - pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 Homozygous PubMed: Pennings 2004 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Pennings 2004 Relative - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1227G>A r.(?) p.(Trp409*) Laminin N-terminal (271-517) Maternal (inferred) - pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 Homozygous PubMed: Pennings 2004 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Pennings 2004 Relative - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1227G>A r.(?) p.(Trp409*) Laminin N-terminal (271-517) Parent #2 - pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 Heterozygous PubMed: Pennings 2004 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Pennings 2004 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1227G>A r.(?) p.(Trp409*) Laminin N-terminal (271-517) Parent #2 - pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 Heterozygous PubMed: Pennings 2004 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Pennings 2004 Relative - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1227G>A r.(?) p.(Trp409*) Laminin N-terminal (271-517) Paternal (inferred) - pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 Homozygous PubMed: Weston 2000 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Weston 2000 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1227G>A r.(?) p.(Trp409*) Laminin N-terminal (271-517) Maternal (inferred) - pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 Homozygous PubMed: Weston 2000 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Weston 2000 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1227G>A r.(?) p.(Trp409*) Laminin N-terminal (271-517) Parent #1 - pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 Heterozygous PubMed: Weston 2000 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Weston 2000 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1227G>A r.(?) p.(Trp409*) Laminin N-terminal (271-517) Parent #1 - pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 Heterozygous PubMed: Pennings 2004(2) - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Pennings 2004(2) Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1227G>A r.(?) p.(Trp409*) Laminin N-terminal (271-517) Parent #2 - pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 Heterozygous PubMed: Pennings 2004(2) - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Pennings 2004(2) Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1227G>A r.(?) p.(Trp409*) Laminin N-terminal (271-517) Parent #2 - pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 Heterozygous PubMed: Pennings 2004(2) - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Pennings 2004(2) Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1227G>A r.(?) p.(Trp409*) Laminin N-terminal (271-517) Paternal (confirmed) - pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 Heterozygous PubMed: Neveling 2012 - - Germline - - none - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Neveling 2012 Proband F - - - - - - - 1 Anne-Françoise Roux
+/. - c.1227G>A r.(?) p.(Trp409Ter) - Unknown - pathogenic g.216497611C>T - USH2A(NM_206933.2):c.1227G>A (p.W409*), USH2A(NM_206933.4):c.1227G>A (p.W409*) - USH2A_000156 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 7 c.1227G>A r.(1227g>a) p.(Trp409*) - Parent #1 ACMG pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W19-0115 Journal: Reurink 2021 - - - - - - - - - 1 Janine Reurink
+/. 7 c.1227G>A r.(1227g>a) p.(Trp409*) - Parent #2 ACMG pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W19-0121 Journal: Reurink 2021 - - - - - - - - - 1 Janine Reurink
+/. - c.1227G>A r.(?) p.(Trp409*) - Parent #1 ACMG pathogenic g.216497611C>T g.216324269C>T USH2A c.1227G>A, p.(Trp409*) - USH2A_000156 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0115 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+/. - c.1227G>A r.(?) p.(Trp409*) - Parent #2 ACMG pathogenic g.216497611C>T g.216324269C>T USH2A c.1227G>A, p.(Trp409*) - USH2A_000156 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0121 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+/. - c.1227G>A r.(?) p.(Trp409Ter) - Unknown ACMG pathogenic g.216497611C>T g.216324269C>T - - USH2A_000156 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S, PP1_P PubMed: Reurink, J. et al., 2021; PubMed: Pennings, R. J. et al., 2004 - rs397517979 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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