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.

8 entries on 1 page. Showing entries 1 - 8.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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P-domain     

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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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Disease     

ID_report     

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Owner     
+/+ 54 c.10612C>T r.(?) p.(Arg3538*) Fibronectin type-III 20 (3499-3585) Unknown - pathogenic g.215955512G>A g.215782170G>A - - USH2A_000902 Heterozygous PubMed: Lenassi 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Lenassi 2015 Proband - - Canada - - - - - 1 Eva Lenassi
+/+ 54 c.10612C>T r.(?) p.(Arg3538*) Fibronectin type-III 20 (3499-3585) Parent #1 - pathogenic g.215955512G>A g.215782170G>A - - USH2A_000902 Heterozygous; mutation PubMed: Jiang 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Jiang 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+/+ 54 c.10612C>T r.(?) p.(Arg3538*) Fibronectin type-III 20 (3499-3585) Parent #2 - pathogenic g.215955512G>A g.215782170G>A - - USH2A_000902 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - Germany - - - - - 1 Crystel Bonnet
?/. - c.10612C>T r.(?) p.(Arg3538*) - Unknown - VUS g.215955512G>A g.215782170G>A - - USH2A_000902 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 10003578 PubMed: Ellingford 2016 patient - - - - - - - - 1 LOVD
+/. 54 c.10612C>T r.(?) p.(Arg3538*) - Unknown ACMG pathogenic g.215955512G>A g.215782170G>A NM_206933.2:c.10612C>T, NP_996816.2:p.(Arg3538Ter), NC_000001.10:g.215955512G>A - USH2A_000902 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - panel of 441 hereditary eye disease genes including 291 genes related to IRD retinal disease 2016121912 PubMed: Wang 2018 - M ? China Han Chinese - - - - 1 LOVD
+/. - c.10612C>T r.(?) p.(Arg3538*) - Unknown - pathogenic g.215955512G>A g.215782170G>A c.10612C>T, p.Arg3538Ter - USH2A_000902 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI726_001443 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+/. 54 c.10612C>T r.(?) p.(Arg3538*) - Parent #1 ACMG pathogenic g.215955512G>A g.215782170G>A USH2A c.C10612T, p.R3538* - USH2A_000902 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease USHsrf7 PubMed: Zhu 2021 family 192, patient USHsrf7 M - China - - - - - 1 LOVD
+/. - c.10612C>T r.(?) p.(Arg3538Ter) - Unknown ACMG pathogenic g.215955512G>A g.215782170G>A - - USH2A_000902 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Lenassi, E. et al., 2015; PubMed: Bonnet, C. et al., 2016; PubMed: Jiang, L. et al., 2015 - rs878853413 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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