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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-?/. - c.3123C>A r.(?) p.(His1041Gln) - Unknown - likely benign g.216390763G>T g.216217421G>T USH2A(NM_206933.2):c.3123C>A (p.H1041Q), USH2A(NM_206933.4):c.3123C>A (p.H1041Q) - USH2A_000929 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/? 15 c.3123C>A r.(?) p.(His1041Gln) Laminin EGF-like 10 (1002-1052) Unknown ACMG likely benign g.216390763G>T g.216217421G>T - - USH2A_000929 Heterozygous PubMed: Bujakowska 2014, USMA missense analysis, missense variant in MSV3d - rs149304901 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bujakowska 2014 Proband - - United States - - - - - 1 Anne-Françoise Roux
-/? 15 c.3123C>A r.(?) p.(His1041Gln) Laminin EGF-like 10 (1002-1052) Unknown ACMG likely benign g.216390763G>T g.216217421G>T - - USH2A_000929 Heterozygous PubMed: Bujakowska 2014, USMA missense analysis, missense variant in MSV3d - rs149304901 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bujakowska 2014 Proband F - United States - - - - - 1 Anne-Françoise Roux
-?/. - c.3123C>A r.(?) p.(His1041Gln) - Unknown - likely benign g.216390763G>T g.216217421G>T USH2A(NM_206933.2):c.3123C>A (p.H1041Q), USH2A(NM_206933.4):c.3123C>A (p.H1041Q) - USH2A_000929 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.3123C>A r.(?) p.(His1041Gln) - Unknown - likely benign g.216390763G>T g.216217421G>T USH2A(NM_206933.2):c.3123C>A (p.H1041Q), USH2A(NM_206933.4):c.3123C>A (p.H1041Q) - USH2A_000929 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.3123C>A r.(?) p.(His1041Gln) - Unknown - VUS g.216390763G>T g.216217421G>T - - USH2A_000929 - PubMed: Wang 2014 - rs149304901 Germline - - - - - DNA SEQ-NG - 66-gene panel retinal disease 7 PubMed: Wang 2014 - F - United States - - - - - 1 LOVD
?/. 15 c.3123C>A r.(?) p.(His1041Gln) - Unknown - VUS g.216390763G>T - c.3123C>A - USH2A_000929 - PubMed: Simpson-2011 - - Germline - 0.30% in 360 controls - - - DNA arraySEQ, PCR, SEQ blood - retinal disease - PubMed: Simpson-2011 - - - United Kingdom (Great Britain) - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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