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     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

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ClinVar ID     

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?/. - c.7379G>A r.(?) p.(Arg2460His) - Unknown - VUS g.216074169C>T g.215900827C>T USH2A(NM_206933.2):c.7379G>A (p.R2460H) - USH2A_000702 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.7379G>A r.(?) p.(Arg2460His) - Unknown - VUS g.216074169C>T g.215900827C>T USH2A(NM_206933.2):c.7379G>A (p.R2460H) - USH2A_000702 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/? 39 c.7379G>A r.(?) p.(Arg2460His) Fibronectin type-III 11 (2435-2528) Parent #1 ACMG likely benign g.216074169C>T g.215900827C>T - - USH2A_000702 Heterozygous; unknown PubMed: Neveling 2012, USMA missense analysis, missense variant in MSV3d - - Germline - - none - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Neveling 2012 Proband F - - - - - - - 1 Anne-Françoise Roux
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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