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.

7 entries on 1 page. Showing entries 1 - 7.
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+?/. - c.10699del r.(?) p.(Leu3567*) - Unknown - likely pathogenic g.215955425del g.215782083del USH2A c.10699del, p.Leu3567Ter - USH2A_002279 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 003-325 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. - c.10699del r.(?) p.(Leu3567*) - Unknown - likely pathogenic g.215955425del g.215782083del c.10699del, p.Leu3567Ter - USH2A_002279 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 001-465 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+/. 54 c.10699del r.(?) p.(Leu3567*) - Unknown - pathogenic (recessive) g.215955425del - c.10699del - USH2A_002279 - PubMed: Colombo-2020 - - Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
+/. 54 c.10699del r.(?) p.(Leu3567*) - Unknown - pathogenic (recessive) g.215955425del - c.10699del - USH2A_002279 - PubMed: Colombo-2020 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
+/. 54 c.10699del r.(?) p.(Leu3567*) - Unknown - pathogenic g.215955425del - c.10699del - USH2A_002279 - PubMed: Colombo-2020 - - Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
+/. - c.10699del r.(?) p.(Leu3567*) - Both (homozygous) - pathogenic g.215955425del g.215782083del USH2A c.10699del, p.(Leu3567*) - USH2A_002279 homozygous PubMed: Falsini 2021 - - Germline yes - - - - DNA SEQ-NG-I - retrospective study (warning: duplicates in database possible) retinal disease 11 PubMed: Falsini 2021 - M - Italy - - - - - 1 LOVD
+/. - c.10699del r.(?) p.(Leu3567Ter) - Unknown ACMG pathogenic g.215955425del g.215782083del 10699delC - USH2A_002279 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Falsini, B. et al., 2021; PubMed: Colombo, L. et al., 2022; PubMed: Colombo, L. et al., 2021 - rs1661659605 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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