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     
?/. 23 c.4821G>C r.(?) p.(Trp1607Cys) - Parent #1 ACMG VUS g.216262419C>G g.216089077C>G USH2A c.4821G>C, p.Trp1607Cys - USH2A_002573 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes USH 6 PubMed: Meng 2020 - M - China - - - - - 1 LOVD
?/. 23 c.4821G>C r.(?) p.(Trp1607Cys) - Parent #1 ACMG VUS g.216262419C>G g.216089077C>G USH2A c.4821G>C, p.Trp1607Cys - USH2A_002573 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes USH 7 PubMed: Meng 2020 - F - China - - - - - 1 LOVD
+?/. - c.4821G>C r.(?) p.(Trp1607Cys) - Parent #1 - likely pathogenic g.216262419C>G g.216089077C>G USH2A c.4821G>C, p.Trp1607Cys - USH2A_002573 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH DTP1908095 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+?/. - c.4821G>C r.(?) p.(Trp1607Cys) - Parent #1 - likely pathogenic g.216262419C>G g.216089077C>G USH2A c.4821G>C, p.Trp1607Cys - USH2A_002573 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH DP19010259 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+?/. - c.4821G>C r.(?) p.(Trp1607Cys) - Parent #2 - likely pathogenic g.216262419C>G g.216089077C>G USH2A c.4821G>C, p.Trp1607Cys - USH2A_002573 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH R0161206600 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+?/. - c.4821G>C r.(?) p.(Trp1607Cys) - Parent #2 - likely pathogenic g.216262419C>G g.216089077C>G USH2A c.4821G>C, p.Trp1607Cys - USH2A_002573 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH R0161206601 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+?/. - c.4821G>C r.(?) p.(Trp1607Cys) - Parent #2 - likely pathogenic g.216262419C>G g.216089077C>G USH2A c.4821G>C, p.Trp1607Cys - USH2A_002573 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH R0161007602 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+?/. - c.4821G>C r.(?) p.(Trp1607Cys) - Parent #2 - likely pathogenic g.216262419C>G g.216089077C>G USH2A c.4821G>C, p.Trp1607Cys - USH2A_002573 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH R0161206803 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+?/. - c.4821G>C r.(?) p.(Trp1607Cys) - Parent #2 - likely pathogenic g.216262419C>G g.216089077C>G USH2A c.4821G>C, p.Trp1607Cys - USH2A_002573 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH R0161206604 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+?/. - c.4821G>C r.(?) p.(Trp1607Cys) - Parent #2 - likely pathogenic g.216262419C>G g.216089077C>G USH2A c.4821G>C, p.Trp1607Cys - USH2A_002573 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH R0161006605 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+?/. 23 c.4821G>C r.(?) p.(Trp1607Cys) - Parent #1 ACMG likely pathogenic g.216262419C>G g.216089077C>G USH2A c.4821G>C, p.W1607C - USH2A_002573 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF_1524 PubMed: Zhu 2021 family 153, patient SRF_1524 F - China - - - - - 1 LOVD
+?/. 23 c.4821G>C r.(?) p.(Trp1607Cys) - Parent #1 ACMG likely pathogenic g.216262419C>G g.216089077C>G USH2A c.4821G>C, p.W1607C - USH2A_002573 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF_1523 PubMed: Zhu 2021 family 153, patient SRF_1523 M - China - - - - - 1 LOVD
+/. - c.4821G>C r.(?) p.(Trp1607Cys) - Unknown ACMG pathogenic g.216262419C>G g.216089077C>G - - USH2A_002573 ACMG GN005 criteria: PM2_P PM3_S PP1_S PP3_P PubMed: Gao, F. J. et al., 2021; PubMed: Meng, X. et al., 2021 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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