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.

6 entries on 1 page. Showing entries 1 - 6.
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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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Template     

Technique     

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Disease     

ID_report     

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Owner     
+?/. - c.12560G>A r.(?) p.(Arg4187His) - Unknown - likely pathogenic (recessive) g.215848693C>T g.215675351C>T - - USH2A_002046 - PubMed: Xu 2014 - rs147304271 Germline - 1/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP331 PubMed: Xu 2014 patient M - China - - - - - 1 LOVD
+/. 63 c.12560G>A r.(?) p.(Arg4187His) - Unknown ACMG pathogenic g.215848693C>T g.215675351C>T NM_206933.2:c.12560G>A, NP_996816.2:p.(Arg4187His), NC_000001.10:g.215848693C>T - USH2A_002046 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - panel of 441 hereditary eye disease genes including 291 genes related to IRD retinal disease 2016082904 PubMed: Wang 2018 - F ? China Han Chinese - - - - 1 LOVD
?/. - c.12560G>A r.(?) p.(Arg4187His) - Paternal (inferred) ACMG VUS g.215848693C>T g.215675351C>T USH2A M4: c.12560G>A;p. Arg4187His - USH2A_002046 heterozygous PubMed: Gonzalez-del Pozo 2020 - rs147304271 Germline yes - - - - DNA SEQ blood - retinal disease III:3 PubMed: Gonzalez-del Pozo 2020 proband F - Spain - - - - - 1 LOVD
+?/. 63 c.12560G>A r.(?) p.(Arg4187His) - Unknown - likely pathogenic (recessive) g.215848693C>T - c.12560G>A - USH2A_002046 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - F - - - - - - - 1 LOVD
?/. - c.12560G>A r.(?) p.(Arg4187His) - Parent #1 - VUS g.215848693C>T g.215675351C>T USH2A c.12560G>A, p.Arg4187His - USH2A_002046 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD17111461 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
?/. - c.12560G>A r.(?) p.(Arg4187His) - Unknown ACMG VUS g.215848693C>T g.215675351C>T - - USH2A_002046 ACMG GN005 criteria: PM2_P PM3_P BP4_P PubMed: Gao, F. J. et al., 2021 - rs147304271 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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