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     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. 41 c.7871C>T r.(?) p.(Pro2624Leu) - Parent #1 - likely pathogenic g.216062120G>A g.215888778G>A - - USH2A_001114 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - Germline - - - - - DNA SEQ-NG - - deafness - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - 1 Mieke Wesdorp
?/. - c.7871C>T r.(?) p.(Pro2624Leu) - Unknown - VUS g.216062120G>A g.215888778G>A - - USH2A_001114 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.7871C>T r.(?) p.(Pro2624Leu) - Parent #1 ACMG likely pathogenic (recessive) g.216062120G>A g.215888778G>A - - USH2A_001114 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19332 PubMed: Sun 2018 family - no China - - - - - 1 LOVD
+?/. 41 c.7871C>T r.(?) p.(Pro2624Leu) - Parent #1 ACMG likely pathogenic g.216062120G>A g.215888778G>A USH2A c.7871C>T, p.P2624L - USH2A_001114 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF833 PubMed: Zhu 2021 family 90, patient SRF833 M - China - - - - - 1 LOVD
?/. - c.7871C>T r.(?) p.(Pro2624Leu) - Unknown ACMG VUS g.216062120G>A g.215888778G>A - - USH2A_001114 ACMG GN005 criteria: PM2_P PM3_M PubMed: Sun, T. et al., 2018 - rs748455430 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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