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.

2 entries on 1 page. Showing entries 1 - 2.
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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     
+?/. - c.2310dup r.(?) p.(Glu771Argfs*8) - Parent #2 - likely pathogenic g.216420431dup g.216247089dup USH2A c.2310_2311insA, p.Glu771Argfs8 - USH2A_002586 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH DP19081631 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+/. - c.2310dup r.(?) p.(Glu771ArgfsTer8) - Unknown ACMG pathogenic g.216420431dup g.216247089dup 2310dupA - USH2A_002586 ACMG GN005 criteria: PVS1_VS PS4_P PP1_S PubMed: Gao, F. J. et al., 2021 - rs2036065933 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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