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.

5 entries on 1 page. Showing entries 1 - 5.
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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     
+/. 63 c.12580T>C r.(?) p.(Cys4194Arg) - Unknown ACMG pathogenic g.215848673A>G g.215675331A>G NM_206933.2:c.12580T>C, NP_996816.2:p.(Cys4194Arg), NC_000001.10:g.215848673A>G - USH2A_002138 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - panel of 441 hereditary eye disease genes including 291 genes related to IRD retinal disease 2016112809 PubMed: Wang 2018 - M ? China Han Chinese - - - - 1 LOVD
+/. 63 c.12580T>C r.(?) p.(Cys4194Arg) - Unknown ACMG pathogenic g.215848673A>G g.215675331A>G NM_206933.2:c.12580T>C, NP_996816.2:p.(Cys4194Arg), NC_000001.10:g.215848673A>G - USH2A_002138 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - panel of 441 hereditary eye disease genes including 291 genes related to IRD retinal disease 2016122601 PubMed: Wang 2018 - M ? China Han Chinese - - - - 1 LOVD
+?/. 63 c.12580T>C r.(?) p.(Cys4194Arg) - Unknown - likely pathogenic (recessive) g.215848673A>G - c.12580T>C - USH2A_002138 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - M - - - - - - - 1 LOVD
?/. 63 c.12580T>C r.(?) p.(Cys4194Arg) - Parent #1 ACMG VUS g.215848673A>G g.215675331A>G USH2A c.12580T>C, p.Cys4194Arg - USH2A_002138 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes retinal disease 53 PubMed: Meng 2020 - M - China - - - - - 1 LOVD
?/. - c.12580T>C r.(?) p.(Cys4194Arg) - Unknown ACMG VUS g.215848673A>G g.215675331A>G - - USH2A_002138 ACMG GN005 criteria: PM2_P PM3_M BP4_P PubMed: Lenassi, E. et al., 2015; PubMed: Meng, X. et al., 2021 - rs769001387 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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