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.

6 entries on 1 page. Showing entries 1 - 6.
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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     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.10576C>T r.(?) p.(Gln3526Ter) - Unknown - pathogenic g.215956089G>A g.215782747G>A - - USH2A_001346 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.10576C>T r.(?) p.(Gln3526Ter) - Unknown ACMG pathogenic g.215956089G>A - - - USH2A_001346 - PubMed: Mansard et al, 2021 - rs773875669 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+/. - c.10576C>T r.(?) p.(Gln3526*) - Parent #1 - pathogenic g.215956089G>A g.215782747G>A USH2A c.10576C>T, p.Gln3526* - USH2A_001346 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD18050569 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+/. 53 c.10576C>T r.(?) p.(Gln3526*) - Parent #2 ACMG pathogenic g.215956089G>A g.215782747G>A USH2A c.10576C>T, p.Q3526* - USH2A_001346 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF682 PubMed: Zhu 2021 family 52, patient SRF682 M - China - - - - - 1 LOVD
+/. 53 c.10576C>T r.(?) p.(Gln3526*) - Parent #2 ACMG pathogenic g.215956089G>A g.215782747G>A USH2A c.10576C>T, p.Gla3526Ter - USH2A_001346 error in annotation p.(Glyln3526Threr) should be p.(Glyln3526Ter) ((p.(Gln3526*)) PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 64 PubMed: Zhu 2021 family 229, patient 64 F - China - - - - - 1 LOVD
+/. - c.10576C>T r.(?) p.(Gln3526Ter) - Unknown ACMG pathogenic g.215956089G>A g.215782747G>A - - USH2A_001346 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Gao, F. J. et al., 2021; PubMed: Mansard, L. et al., 2021 - rs773875669 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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