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.

15 entries on 1 page. Showing entries 1 - 15.
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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     

Country     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 69 c.14977_14978del r.(?) p.(Phe4993Profs*7) Fibronectin type-III 35 (4928-5014) Paternal (confirmed) - pathogenic g.215812574_215812575del g.215639232_215639233del 14977_14978delTT - USH2A_000272 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 69 c.14977_14978del r.(?) p.(Phe4993Profs*7) Fibronectin type-III 35 (4928-5014) Parent #2 - pathogenic g.215812574_215812575del g.215639232_215639233del 14977_14978delTT - USH2A_000272 Heterozygous PubMed: Sodi 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Sodi 2014 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 69 c.14977_14978del r.(?) p.(Phe4993Profs*7) Fibronectin type-III 35 (4928-5014) Paternal (inferred) - pathogenic g.215812574_215812575del g.215639232_215639233del 14977_14978delTT - USH2A_000272 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Italy - - - - - 1 Crystel Bonnet
+/+ 69 c.14977_14978del r.(?) p.(Phe4993Profs*7) Fibronectin type-III 35 (4928-5014) Maternal (inferred) - pathogenic g.215812574_215812575del g.215639232_215639233del 14977_14978delTT - USH2A_000272 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Italy - - - - - 1 Crystel Bonnet
+/+ 69 c.14977_14978del r.(?) p.(Phe4993Profs*7) Fibronectin type-III 35 (4928-5014) Parent #1 - pathogenic g.215812574_215812575del g.215639232_215639233del 14977_14978delTT - USH2A_000272 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - Italy - - - - - 1 Crystel Bonnet
+/+ 69 c.14977_14978del r.(?) p.(Phe4993Profs*7) Fibronectin type-III 35 (4928-5014) Paternal (inferred) - pathogenic g.215812574_215812575del g.215639232_215639233del 14977_14978delTT - USH2A_000272 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Italy - - - - - 1 Crystel Bonnet
+/+ 69 c.14977_14978del r.(?) p.(Phe4993Profs*7) Fibronectin type-III 35 (4928-5014) Maternal (inferred) - pathogenic g.215812574_215812575del g.215639232_215639233del 14977_14978delTT - USH2A_000272 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Italy - - - - - 1 Crystel Bonnet
+?/+ - c.14977_14978del r.(?) p.(Phe4993Profs*7) - Unknown ACMG likely pathogenic g.215812574_215812575del g.215639232_215639233del - - USH2A_000272 - PubMed: Karali 2019, Journal: Karali 2019 - - Germline yes - - - - DNA SEQ-NG - clinical exome sequencing retinal disease Fam8P10 PubMed: Karali 2019, Journal: Karali 2019 family, 2 affected - - Italy - - - - - 2 Sandro Banfi
+/. - c.14977_14978del r.(?) p.(Phe4993Profs * 7) - Parent #2 - pathogenic (recessive) g.215812574_215812575del g.215639232_215639233del - - USH2A_000272 - PubMed: Karali 2019, Journal: Karali 2019 - - Germline - - - - - DNA SEQ-NG - - retinal disease Fam8P11 PubMed: Karali 2019, Journal: Karali 2019 - - - Italy - - - - - 1 Sandro Banfi
+?/. - c.14977_14978del r.(?) p.(Phe4993Profs*7) - Parent #2 - likely pathogenic (recessive) g.215812574_215812575del g.215639232_215639233del - - USH2A_000272 - PubMed: Eandi 2017 - - Germline - - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam7PatTO8 PubMed: Eandi 2017 - M - Italy - - - - - 1 LOVD
+?/. - c.14977_14978del r.(?) p.(Phe4993Profs*7) - Parent #2 - likely pathogenic (recessive) g.215812574_215812575del g.215639232_215639233del 14977_14987del (Phe4993Profs*7) - USH2A_000272 - PubMed: Eandi 2017 - - Germline - - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam11PatTO14 PubMed: Eandi 2017 - M - Italy - - - - - 1 LOVD
+/. 69 c.14977_14978del r.(?) p.(Phe4993Profs*7) - Unknown - pathogenic g.215812571_215812572del - c.14977_14978del - USH2A_000272 - PubMed: Colombo-2020 - rs747160949 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
+/. 69 c.14977_14978del r.(?) p.(Phe4993Profs*7) - Unknown - pathogenic g.215812571_215812572del - c.14977_14978del - USH2A_000272 - PubMed: Colombo-2020 - rs747160949 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+/. - c.14977_14978del r.(?) p.(Phe4993ProfsTer7) - Unknown ACMG pathogenic g.215812574_215812575del g.215639232_215639233del 14977_14978delTT - USH2A_000272 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Bonnet, C. et al., 2016; PubMed: Colombo, L. et al., 2022; PubMed: Colombo, L. et al., 2022; PubMed: Karali, M. et al., 2019; PubMed: Colombo, L. et al., 2021; PubMed: Eandi, C. M. et al., 2017 - rs747160949 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. 69 c.14977_14978delTT r.(?) p.(Phe4993Profs*7) - Both (homozygous) - pathogenic g.215812574_215812575del g.215639232_215639233del c.14977_14978delTT - USH2A_000272 - PubMed: Bernardis 2016 - - Germline - - - - - DNA SEQ-NG - 72-gene panel retinal disease IRD084 PubMed: Bernardis 2016 - - Italy - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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