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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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Reference     

ClinVar ID     

dbSNP ID     

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Disease     

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Owner     
+/. - c.2414G>C r.(?) p.(Gly805Ala) - Unknown - pathogenic g.216420322C>G g.216246980C>G - - USH2A_001539 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs587783023 Germline - 8/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 8 Yoshito Koyanagi
?/. 13 c.2414G>C r.(?) p.(Gly805Ala) - Unknown - VUS g.216420322C>G g.216246980C>G G2414C - USH2A_001539 - PubMed: Katagiri 2014 - - Germline - - - - - DNA SEQ-NG - WES retinal disease RP#027 PubMed: Katagiri 2014 family - - Japan - - - - - 1 LOVD
?/. - c.2414G>C r.(?) p.(Gly805Ala) - Unknown ACMG VUS g.216420322C>G g.216246980C>G USH2A c.G2414C, p.G805A - USH2A_001539 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 7 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
?/. - c.2414G>C r.(?) p.(Gly805Ala) - Unknown ACMG VUS g.216420322C>G g.216246980C>G USH2A c.G2414C, p.G805A - USH2A_001539 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 2 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
?/. - c.2414G>C r.(?) p.(Gly805Ala) - Unknown ACMG VUS g.216420322C>G g.216246980C>G - - USH2A_001539 ACMG GN005 criteria: PM2_P PubMed: Ma, D. J. et al., 2021 - rs587783023 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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