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.

3 entries on 1 page. Showing entries 1 - 3.
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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)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

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Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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VIP     

Data_av     

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Owner     
+/. - c.10820A>C r.(?) p.(His3607Pro) - Parent #1 - pathogenic (recessive) g.215953304T>G g.215779962T>G - - USH2A_001909 - PubMed: Villanueva 2018 - - Germline - - - - - DNA SEQ-NG - 233-gene panel retinal disease RD1 PubMed: Villanueva 2018 2-generation family, 1 affected, unaffected parents M - - - - - - - 1 LOVD
+/. - c.10820A>C r.(?) p.(His3607Pro) - Unknown ACMG pathogenic g.215953304T>G - - - USH2A_001909 - Villafuerte-de la Cruz RA, et al., 2023. Submitted ClinVar-438200 rs750321557 Germline yes - - - - DNA SEQ-NG-I BUCCAL SWAB - retinitis pigmentosa, X-linked, and sinorespiratory infections, with/without deafness 3831892 Villafuerte-de la Cruz RA, et al., 2023. Submitted - M no Mexico Hispanic - - - none 1 Rocio Villafuerte-de la Cruz
?/. - c.10820A>C r.(?) p.(His3607Pro) - Unknown ACMG VUS g.215953304T>G g.215779962T>G - - USH2A_001909 ACMG GN005 criteria: PM2_P PM3_M PP1_P PubMed: Villanueva, A. et al., 2018 - rs750321557 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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