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.

4 entries on 1 page. Showing entries 1 - 4.
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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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Re-site     

VIP     

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Disease     

ID_report     

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Owner     
-?/? 18 c.3840G>C r.(?) p.(Met1280Ile) Fibronectin type-III 3 (1242-1357) Unknown ACMG likely benign g.216371898C>G g.216198556C>G - - USH2A_000630 Heterozygous; UV4 PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - - +Hpy188I;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/. - c.3840G>C r.(?) p.(Met1280Ile) - Parent #2 - likely pathogenic g.216371898C>G g.216198556C>G USH2A c.3840G>C - USH2A_000630 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 13 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.3840G>C r.(?) p.(Met1280Ile) - Parent #2 - likely pathogenic g.216371898C>G g.216198556C>G USH2A c.3840G>C - USH2A_000630 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 19 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
?/. - c.3840G>C r.(?) p.(Met1280Ile) - Unknown ACMG VUS g.216371898C>G g.216198556C>G - - USH2A_000630 ACMG GN005 criteria: PM2_P PM3_P PubMed: Le Quesne Stabej, P. et al., 2012 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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