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.

13 entries on 1 page. Showing entries 1 - 13.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.14017T>C r.(?) p.(Tyr4673His) - Unknown - pathogenic g.215844430A>G g.215671088A>G - - USH2A_001460 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - - Germline - 4/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 4 Yoshito Koyanagi
?/. - c.14017T>C r.(?) p.(Tyr4673His) - Unknown - VUS g.215844430A>G g.215671088A>G - - USH2A_001460 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.14017T>C r.(?) p.(Tyr4673His) - Parent #2 - likely pathogenic (recessive) g.215844430A>G g.215671088A>G - - USH2A_001460 - PubMed: Huang 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease QT739 PubMed: Huang 2016 - - - China - - - - - 1 Johan den Dunnen
?/. - c.14017T>C r.(?) p.(Tyr4673His) - Unknown ACMG VUS g.215844430A>G g.215671088A>G USH2A c.T14017C, p.Y4673H - USH2A_001460 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 121 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
+?/. 64 c.14017T>C r.(?) p.(Tyr4673His) - Unknown - likely pathogenic (recessive) g.215844430A>G - c.14017T>C - USH2A_001460 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - M - - - - - - - 1 LOVD
+?/. 64 c.14017T>C r.(?) p.(Tyr4673His) - Unknown - likely pathogenic (recessive) g.215844430A>G - c.14017T>C - USH2A_001460 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - F - - - - - - - 1 LOVD
+?/. 64 c.14017T>C r.(?) p.(Tyr4673His) - Unknown - likely pathogenic (recessive) g.215844430A>G - c.14017T>C - USH2A_001460 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - M - - - - - - - 1 LOVD
?/. 64 c.14017T>C r.(?) p.(Tyr4673His) - Parent #2 ACMG VUS g.215844430A>G g.215671088A>G USH2A c.14017T>C, p.Tyr4673His - USH2A_001460 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes USH 5 PubMed: Meng 2020 - M - China - - - - - 1 LOVD
+/. - c.14017T>C r.(?) p.(Tyr4673His) - Parent #2 - pathogenic g.215844430A>G g.215671088A>G USH2A c.14017T>C, p.Tyr4673His - USH2A_001460 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD17043134 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+?/. 64 c.14017T>C r.(?) p.(Tyr4673His) - Parent #1 ACMG likely pathogenic g.215844430A>G g.215671088A>G USH2A c.14017T>C, p.Y4673H - USH2A_001460 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 43665347 PubMed: Zhu 2021 family 60, patient 43665347 M - China - - - - - 1 LOVD
+?/. 64 c.14017T>C r.(?) p.(Tyr4673His) - Paternal (confirmed) ACMG likely pathogenic g.215844430A>G g.215671088A>G M2: USH2A c.14017T>C, Y4673H - USH2A_001460 heterozygous PubMed: Chen 2020 - - Germline ? - - - - DNA SEQ-NG-I blood xGen Exome Research Panel retinal disease 1-II:2 PubMed: Chen 2020 family 1, proband F - China - - - - - 1 LOVD
+?/. 64 c.14017T>C r.(?) p.(Tyr4673His) - Paternal (confirmed) ACMG likely pathogenic g.215844430A>G g.215671088A>G M2: USH2A c.14017T>C, Y4673H - USH2A_001460 heterozygous PubMed: Chen 2020 - - Germline yes - - - - DNA SEQ-NG-I blood xGen Exome Research Panel retinal disease 1-II:3 PubMed: Chen 2020 family 1, brother of proband M - China - - - - - 1 LOVD
?/. - c.14017T>C r.(?) p.(Tyr4673His) - Unknown ACMG VUS g.215844430A>G g.215671088A>G - - USH2A_001460 ACMG GN005 criteria: PM2_P PM3_P PubMed: Gao, F. J. et al., 2021; PubMed: Ma, D. J. et al., 2021; PubMed: Meng, X. et al., 2021 - rs1040917329 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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