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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Effect     

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AscendingDNA change (cDNA)     

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+/+ 50 c.9811del r.(?) p.(Met3271Cysfs*30) Cystein rich (3192-3358) Parent #1 - pathogenic g.215972397del g.215799055del - - USH2A_000914 Heterozygous PubMed: Sodi 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Sodi 2014 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 50 c.9811del r.(?) p.(Met3271Cysfs*30) Cystein rich (3192-3358) Parent #1 - pathogenic g.215972397del g.215799055del - - USH2A_000914 Heterozygous PubMed: Sodi 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Sodi 2014 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 50 c.9811del r.(?) p.(Met3271Cysfs*30) Cystein rich (3192-3358) Parent #2 - pathogenic g.215972397del g.215799055del - - USH2A_000914 Heterozygous PubMed: Sodi 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Sodi 2014 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 50 c.9811del r.(?) p.(Met3271Cysfs*30 Cystein rich (3192-3358) Paternal (confirmed) - pathogenic g.215972397del g.215799055del 9811delA - USH2A_000914 Heterozygous; UV3 PubMed: Lenarduzzi 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Lenarduzzi 2015 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 50 c.9811del r.(?) p.(Met3271Cysfs*30) Cystein rich (3192-3358) Parent #2 - pathogenic g.215972397del g.215799055del 9811delA - USH2A_000914 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - Italy - - - - - 1 Crystel Bonnet
+/. 50 c.9811del r.(?) p.(Met3271Cysfs*30) - Unknown - pathogenic g.215972396del - c.9811del - USH2A_000914 - PubMed: Colombo-2020 - rs767328784 Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
+/. - c.9811del r.(?) p.(Met3271CysfsTer30) - Unknown ACMG pathogenic g.215972397del g.215799055del 9811delA - USH2A_000914 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Bonnet, C. et al., 2016; PubMed: Colombo, L. et al., 2022; PubMed: Colombo, L. et al., 2021 - rs767328784 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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