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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?/? 20 c.4378G>A r.(?) p.(Gly1460Arg) - Unknown - VUS g.216363583C>T g.216190241C>T - - USH2A_000891 - - - - Unknown - - - - - DNA SEQ-NG-I - - RP - - - - - (United States) - - - - - 1 Feng Wang
+?/? 20 c.4378G>A r.(?) p.(Gly1460Arg) Fibronectin type-III 4 (1367-1462) Unknown ACMG VUS g.216363583C>T g.216190241C>T - - USH2A_000891 Heterozygous PubMed: Lenassi 2015, USMA missense analysis, missense variant in MSV3d - rs139311927 Germline - - - - - DNA SEQ - - RPar - PubMed: Lenassi 2015 Proband - - Canada - - - - - 1 Eva Lenassi
?/. - c.4378G>A r.(?) p.(Gly1460Arg) - Unknown - VUS g.216363583C>T - USH2A(NM_206933.4):c.4378G>A (p.G1460R) - USH2A_000891 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 20 c.4378G>A r.(?) p.(Gly1460Arg) - Unknown - pathogenic g.216363583C>T - c.4378G>A - USH2A_000891 - PubMed: Wang-2014 - - Germline - - - - - DNA PCR, SEQ-NG blood or a saliva sample - retinal disease - PubMed: Wang-2014 - - no - - - - - - 1 LOVD
+?/. 20 c.4378G>A r.(?) p.(Gly1460Arg) - Parent #2 ACMG likely pathogenic g.216363583C>T g.216190241C>T USH2A c.4378G>A, p.G1460R - USH2A_000891 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF833 PubMed: Zhu 2021 family 90, patient SRF833 M - China - - - - - 1 LOVD
?/. - c.4378G>A r.(?) p.(Gly1460Arg) - Unknown - VUS g.216363583C>T - USH2A(NM_206933.4):c.4378G>A (p.G1460R) - USH2A_000891 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.4378G>A r.(?) p.(Gly1460Arg) - Unknown ACMG VUS g.216363583C>T g.216190241C>T - - USH2A_000891 ACMG GN005 criteria: PM2_P PM3_M PubMed: Lenassi, E. et al., 2015 - rs139311927 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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