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.

8 entries on 1 page. Showing entries 1 - 8.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

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Reference     

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Disease     

ID_report     

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Owner     
+?/. 25 c.5018T>C r.(?) p.(Leu1673Pro) - Parent #1 - likely pathogenic g.216258189A>G g.216084847A>G - - USH2A_001113 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - Germline - - - - - DNA SEQ-NG - - deafness - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - 1 Mieke Wesdorp
?/. 25 c.5018T>C r.(?) p.(Leu1673Pro) - Unknown - VUS g.216258189A>G g.216084847A>G - - USH2A_001113 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - Germline - - - - - DNA SEQ-NG - - deafness - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - 1 Mieke Wesdorp
?/. - c.5018T>C r.(?) p.(Leu1673Pro) - Unknown - VUS g.216258189A>G g.216084847A>G USH2A(NM_206933.2):c.5018T>C (p.L1673P), USH2A(NM_206933.4):c.5018T>C (p.L1673P) - USH2A_001113 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.5018T>C r.(?) p.(Leu1673Pro) - Unknown - VUS g.216258189A>G g.216084847A>G USH2A(NM_206933.2):c.5018T>C (p.L1673P), USH2A(NM_206933.4):c.5018T>C (p.L1673P) - USH2A_001113 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.5018T>C r.(?) p.(Leu1673Pro) - Unknown - pathogenic g.216258189A>G g.216084847A>G USH2A(NM_206933.2):c.5018T>C (p.L1673P), USH2A(NM_206933.4):c.5018T>C (p.L1673P) - USH2A_001113 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. 25 c.5018T>C r.(?) p.(Leu1673Pro) - Unknown - likely pathogenic g.216258189A>G - p.L1673P - USH2A_001113 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 25 c.5018T>C r.(?) p.(Leu1673Pro) - Unknown - likely pathogenic g.216258189A>G - p.L1673P - USH2A_001113 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
?/. - c.5018T>C r.(?) p.(Leu1673Pro) - Unknown ACMG VUS g.216258189A>G g.216084847A>G - - USH2A_001113 ACMG GN005 criteria: PM2_P PM3_P PP3_P PubMed: Wafa, T. T. et al., 2021 - rs1162305984 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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