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.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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ISCN     

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Reference     

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Owner     
+/+ 28 c.5735_5736del r.(?) p.(Lys1912Argfs*24) Fibronectin type-III 5 (1871-1949) Parent #2 - pathogenic g.216246481_216246482del g.216073139_216073140del 5735_5736del - p.1912_1912del - USH2A_000956 Heterozygous; mutation PubMed: Jiang 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Jiang 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+/+ 28 c.5735_5736del r.(?) p.(Lys1912Argfs*24) Fibronectin type-III 5 (1871-1949) Parent #1 - pathogenic g.216246481_216246482del g.216073139_216073140del 5735_5736del - p.1912_1912del - USH2A_000956 Heterozygous; mutation PubMed: Jiang 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Jiang 2015 Proband F - China - - - - - 1 Anne-Françoise Roux
+/. - c.5735_5736del r.(?) p.(Lys1912Argfs*24) - Parent #1 ACMG pathogenic (recessive) g.216246481_216246482del g.216073139_216073140del c.5735_5736delAA - USH2A_000956 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19736 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+/. - c.5735_5736del r.(?) p.(Lys1912Argfs*24) - Parent #1 ACMG pathogenic g.216246481_216246482del g.216073139_216073140del USH2A c.5735_5736del, p.(Lys1912Argfs*24) - USH2A_000956 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease USHsrf55 PubMed: Zhu 2021 family 213, patient USHsrf55 F - China - - - - - 1 LOVD
+/. - c.5735_5736del r.(?) p.(Lys1912Argfs*24) - Parent #2 ACMG pathogenic g.216246481_216246482del g.216073139_216073140del USH2A c.5735_5736del, p.(Lys1912Argfs*24) - USH2A_000956 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease USHsrf10 PubMed: Zhu 2021 family 194, patient USHsrf10 M - China - - - - - 1 LOVD
+/. - c.5735_5736del r.(?) p.(Lys1912ArgfsTer24) - Unknown ACMG pathogenic g.216246481_216246482del g.216073139_216073140del 5735_5736delAA - USH2A_000956 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Sun, T. et al., 2018; PubMed: Jiang, L. et al., 2015 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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