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.

5 entries on 1 page. Showing entries 1 - 5.
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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     

Remarks     

Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
+/+ 35 c.6752C>A r.(?) p.(Ser2251*) Fibronectin type-III 9 (2241-2325) Parent #2 - pathogenic g.216166415G>T g.215993073G>T - - USH2A_000963 Heterozygous; mutation PubMed: Jiang 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Jiang 2015 Proband F - China - - - - - 1 Anne-Françoise Roux
+/+ 35 c.6752C>A r.(?) p.(Ser2251*) Fibronectin type-III 9 (2241-2325) Parent #1 - pathogenic g.216166415G>T g.215993073G>T - - USH2A_000963 Heterozygous; mutation PubMed: Jiang 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Jiang 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+/. 35 c.6752C>A r.(?) p.(Ser2251*) - Parent #1 ACMG pathogenic g.216166415G>T g.215993073G>T USH2A c.6752C>A, p.S2251* - USH2A_000963 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease USHsrf25 PubMed: Zhu 2021 family 200, patient USHsrf25 M - China - - - - - 1 LOVD
+/. 35 c.6752C>A r.(?) p.(Ser2251*) - Parent #2 ACMG pathogenic g.216166415G>T g.215993073G>T USH2A c.6752C>A, p.S2251* - USH2A_000963 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease USHsrf24 PubMed: Zhu 2021 family 200, patient USHsrf24 F - China - - - - - 1 LOVD
+/. 35 c.6752C>A r.(?) p.(Ser2251*) - Parent #2 ACMG pathogenic g.216166415G>T g.215993073G>T USH2A c.6752C>A, p.S2251* - USH2A_000963 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease AXLM_18 PubMed: Zhu 2021 family 78, patient AXLM_18 F - China - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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