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.

8 entries on 1 page. Showing entries 1 - 8.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

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Variant remarks     

Reference     

ClinVar ID     

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Disease     

ID_report     

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Owner     
+?/? 61 c.11806A>C r.(?) p.(Thr3936Pro) Fibronectin type-III 24 (3863-3960) Parent #2 ACMG VUS g.215901632T>G g.215728290T>G - - USH2A_000002 Heterozygous PubMed: Dai 2008, USMA missense analysis, missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ - - USH2 - PubMed: Dai 2008 Proband M - China - - - - - 1 Anne-Françoise Roux
+/. - c.11806A>C r.(?) p.(Thr3936Pro) - Parent #2 ACMG pathogenic (recessive) g.215901632T>G g.215728290T>G - - USH2A_000002 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ - - HL 73021 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+/. 61 c.11806A>C r.(?) p.(Thr3936Pro) - Unknown ACMG pathogenic g.215901632T>G g.215728290T>G NM_206933.2:c.11806A>C, NP_996816.2:p.(Thr3936Pro), NC_000001.10:g.215901632T>G - USH2A_000002 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - exome sequencing retinal disease 2016092601 PubMed: Wang 2018 - F ? China Han Chinese - - - - 1 LOVD
+?/. 61 c.11806A>C r.(?) p.(Thr3936Pro) - Unknown - likely pathogenic (recessive) g.215901632T>G - c.11806A>C - USH2A_000002 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - WES retinal disease - PubMed: Liu-2020 - F - - - - - - - 1 LOVD
+?/. 61 c.11806A>C r.(?) p.(Thr3936Pro) - Both (homozygous) - likely pathogenic (recessive) g.215901632T>G - c.118036A>C - USH2A_000002 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - F - - - - - - - 1 LOVD
?/. 61 c.11806A>C r.(?) p.(Thr3936Pro) - Both (homozygous) ACMG VUS g.215901632T>G g.215728290T>G USH2A c.11806A>C, p.Thr3936Pro - USH2A_000002 homozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes USH 28 PubMed: Meng 2020 - F - China - - - - - 1 LOVD
+/. - c.11806A>C r.(?) p.(Thr3936Pro) - Parent #1 - pathogenic g.215901632T>G g.215728290T>G USH2A c.11806A>C, p.Thr3936Pro - USH2A_000002 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD18012995 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
?/. - c.11806A>C r.(?) p.(Thr3936Pro) - Unknown ACMG VUS g.215901632T>G g.215728290T>G - - USH2A_000002 ACMG GN005 criteria: PM2_P PM3_S PubMed: Gao, F. J. et al., 2021; PubMed: Sun, T. et al., 2018; PubMed: Meng, X. et al., 2021 - rs2102713705 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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