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.

3 entries on 1 page. Showing entries 1 - 3.
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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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 42 c.8435_8438del r.(?) p.(Thr2812Metfs*17) Fibronectin type-III 14 (2724-2812) Parent #1 - pathogenic g.216052232_216052235del g.215878890_215878893del 8435_8438delCCTA - USH2A_000180 Heterozygous PubMed: Aller 2006 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Aller 2006 Proband F - Spain - - - - - 1 Jose Maria Millan
+?/. - c.8435_8438del r.(?) p.(Thr2812Metfs*17) - Paternal (confirmed) - likely pathogenic g.216052232_216052235del g.215878890_215878893del - - USH2A_000180 - PubMed: Perez-Carro 2018 - - Germline yes - - - - DNA SEQ blood - retinal disease RP-0810 PubMed: Perez-Carro 2018 family RP-0810c F no Spain - - - - - 1 LOVD
+/. - c.8435_8438del r.(?) p.(Thr2812MetfsTer17) - Unknown ACMG pathogenic g.216052232_216052235del g.215878890_215878893del 8435_8438delCCTA - USH2A_000180 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Perez-Carro, R. et al., 2018; PubMed: Aller, E. et al., 2006 - rs1664838877 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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