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     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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VIP     

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Disease     

ID_report     

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Owner     
-?/? 50i c.9959-11T>G r.(?) p.(?) - Unknown ACMG likely benign g.215963635A>C g.215790293A>C - - USH2A_000312 Heterozygous PubMed: Baux 2014 - rs116150014 Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - Cameroon - - - - - 1 Anne-Françoise Roux
-/. - c.9959-11T>G r.(=) p.(=) - Unknown - benign g.215963635A>C g.215790293A>C USH2A(NM_206933.4):c.9959-11T>G - USH2A_000312 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.9959-11T>G r.(?) p.(?) - Both (homozygous) - likely pathogenic g.215963635A>C g.215790293A>C USH2A c.9959-11T>G, p.(?) - USH2A_000312 homozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 112 PubMed: Jauregui 2020 - M - (United States) African American - - - - 1 LOVD
-/. - c.9959-11T>G r.(?) p.(=) - Unknown ACMG benign g.215963635A>C g.215790293A>C - - USH2A_000312 ACMG GN005 criteria: BA1 BS2_S PubMed: Jauregui, R. et al., 2020 - rs116150014 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.9959-11T>G r.(=) p.(=) - Unknown - benign g.215963635A>C - USH2A(NM_206933.4):c.9959-11T>G - USH2A_000312 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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