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.

10 entries on 1 page. Showing entries 1 - 10.
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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     

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Template     

Technique     

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Disease     

ID_report     

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Owner     
+/. - c.15233C>G r.(?) p.(Pro5078Arg) - Unknown - pathogenic g.215807865G>C g.215634523G>C - - USH2A_001455 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs527236122 Germline - 13/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 13 Yoshito Koyanagi
+?/. - c.15233C>G r.(?) p.(Pro5078Arg) - Both (homozygous) - likely pathogenic g.215807865G>C g.215634523G>C - - USH2A_001455 - PubMed: Oishi 2014 - - Germline - - - - - DNA SEQ-NG - 193-gene panel retinal disease K1622 PubMed: Oishi 2014 family - - Japan - - - - - 1 LOVD
+?/. - c.15233C>G r.(?) p.(Pro5078Arg) - Unknown ACMG VUS g.215807865G>C - - - USH2A_001455 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - RP IR_SH_0024 - - F - Korea, South (Republic) - - - - - 1 Jinu Han
+?/. - c.15233C>G r.(?) p.(Pro5078Arg) - Unknown - likely pathogenic g.215807865G>C g.215634523G>C USH2A p.(Pro5078Arg) - USH2A_001455 only protein changes written in the publication; Mutalyzer Back Translator used for coding DNA variant (impossible in case of frameshift mutations); compound heterozygous PubMed: Koyanagi 2020 - - Unknown ? - - - - DNA ? - retrospective study retinal disease OPH-570 PubMed: Koyanagi 2020 - M - Japan - - - - - 1 LOVD
+?/. - c.15233C>G r.(?) p.(Pro5078Arg) - Unknown ACMG likely pathogenic g.215807865G>C g.215634523G>C USH2A c.C15233G, p.P5078R - USH2A_001455 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 126 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
-?/. - c.15233C>G r.(?) p.(Pro5078Arg) - Unknown ACMG likely benign g.215807865G>C g.215634523G>C USH2A c.C15233G, p.P5078R - USH2A_001455 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 127 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
?/. - c.15233C>G r.(?) p.(Pro5078Arg) - Unknown ACMG VUS g.215807865G>C g.215634523G>C USH2A c.C15233G, p.P5078R - USH2A_001455 marked as possibly causative, single heterozygous change in a recessive gene, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 150 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
+?/. - c.15233C>G r.(?) p.(Pro5078Arg) - Parent #2 - likely pathogenic g.215807865G>C g.215634523G>C USH2A c.15233C>G, p.(Pro5078Arg) - USH2A_001455 heterozygous PubMed: Inaba 2020 - - Unknown ? - - - - DNA SEQ-NG-I - panel of 39 (238 patients) or 50 (287 patients) genes retinal disease - PubMed: Inaba 2020 - - - Japan - - - - - 1 LOVD
+?/. - c.15233C>G r.(?) p.(Pro5078Arg) - Parent #2 - likely pathogenic g.215807865G>C g.215634523G>C USH2A c.15233C>G, p.(Pro5078Arg) - USH2A_001455 heterozygous PubMed: Inaba 2020 - - Unknown ? - - - - DNA SEQ-NG-I - panel of 39 (238 patients) or 50 (287 patients) genes retinal disease - PubMed: Inaba 2020 - - - Japan - - - - - 1 LOVD
?/. - c.15233C>G r.(?) p.(Pro5078Arg) - Unknown ACMG VUS g.215807865G>C g.215634523G>C - - USH2A_001455 ACMG GN005 criteria: PM2_P PM3_P PP1_P PubMed: Ma, D. J. et al., 2021; PubMed: Inaba, A. et al., 2020 - rs527236122 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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