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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AscendingDNA change (cDNA)     

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-?/. - c.13709G>A r.(?) p.(Arg4570His) - Unknown - likely benign g.215847544C>T g.215674202C>T USH2A(NM_206933.2):c.13709G>A (p.R4570H), USH2A(NM_206933.4):c.13709G>A (p.R4570H) - USH2A_000442 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.13709G>A r.(?) p.(Arg4570His) - Unknown - likely benign g.215847544C>T g.215674202C>T USH2A(NM_206933.2):c.13709G>A (p.R4570H), USH2A(NM_206933.4):c.13709G>A (p.R4570H) - USH2A_000442 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/? 63 c.13709G>A r.(?) p.(Arg4570His) Fibronectin type-III 31 (4529-4627) Unknown ACMG likely benign g.215847544C>T g.215674202C>T - - USH2A_000442 Heterozygous; benign PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - rs730254 Germline - - - - - DNA SEQ - - USH2 - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
-?/? 63 c.13709G>A r.(?) p.(Arg4570His) Fibronectin type-III 31 (4529-4627) Unknown ACMG likely benign g.215847544C>T g.215674202C>T - - USH2A_000442 Heterozygous; benign PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - rs730254 Germline - - - - - DNA SEQ - - RPar - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
?/. - c.13709G>A r.(?) p.(Arg4570His) - Unknown - VUS g.215847544C>T g.215674202C>T - - USH2A_000442 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs730254 Germline - 1/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 1 Yoshito Koyanagi
?/. - c.13709G>A r.(?) p.(Arg4570His) - Unknown - VUS g.215847544C>T g.215674202C>T - - USH2A_000442 - PubMed: Bryant 2018 - rs730254 Germline - - - - - DNA SEQ-NG - WES retinal disease JB284 PubMed: Bryant 2018 - - - United States - - - - - 1 LOVD
?/. - c.13709G>A r.(?) p.(Arg4570His) - Unknown - VUS g.215847544C>T g.215674202C>T - - USH2A_000442 - PubMed: Bryant 2018 - rs730254 Germline - - - - - DNA SEQ-NG - WES retinal disease JB284 PubMed: Bryant 2018 - - - United States - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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