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.

22 entries on 1 page. Showing entries 1 - 22.
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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     
+/. 2 c.236_239dup r.(?) p.(Gln81Tyrfs*28) - Maternal (confirmed) - pathogenic g.216595440_216595443dup g.216422098_216422101dup 239–242insGTAC (Thr80fs) - USH2A_000135 - PubMed: Behar 2014, Journal: Behar 2014 - - Germline yes - - - - DNA SEQ-NG-I blood - USH2A - PubMed: Behar 2014, Journal: Behar 2014 3-generation family, 2 affecteds (F, M), unaffected carrier parents/sibs; family segregates GJB2 and USH2A variants F;M no Israel Iraq;Jewish;Jewish-Ashkenazi - - - - 3 Zippi Brownstein
+/. 2 c.236_239dup r.(?) p.(Gln81Tyrfs*28) - Both (homozygous) - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 - Sharon, submitted - - Germline - - - - - DNA SEQ - - USH1 - Sharon, submitted - F yes Israel Jewish-Oriental - - - - 2 Dror Sharon
+/. 2 c.236_239dup r.(?) p.(Gln81Tyrfs*28) - Maternal (confirmed) - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 - Sharon, submitted - - Germline - - - - - DNA SEQ - - USH1 - Sharon, submitted - F no Israel Jewish-Oriental - - - - 3 Dror Sharon
+/. 2 c.236_239dup r.(?) p.(Gln81Tyrfs*28) - Paternal (confirmed) - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 - Sharon, submitted - - Germline - - - - - DNA SEQ - - USH1 - Sharon, submitted - F no Israel Jewish-Oriental - - - - 2 Dror Sharon
+/. 2 c.236_239dup r.(?) p.(Gln81Tyrfs*28) - Unknown - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 - Sharon, submitted - - Germline - - - - - DNA SEQ - - USH1 - Sharon, submitted - F yes Israel Yemenite;Jewish - - - - 2 Dror Sharon
+/. 2 c.236_239dup r.(?) p.(Gln81Tyrfs*28) - Unknown - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 - PubMed: Sharon 2019 - - Germline - - - - - DNA SEQ - - retinal disease MOL1141 PubMed: Sharon 2019 - M no Israel Jewish-Oriental - - - - 1 Dror Sharon
+/. 2 c.236_239dup r.(?) p.(Gln81Tyrfs*28) - Unknown - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 - Sharon, submitted - - Germline - - - - - DNA SEQ - - retinal disease - Sharon, submitted - M no Israel Jewish - - - - 1 Dror Sharon
+/+ 2 c.236_239dup r.(?) p.(Thr80Serfs*29) - Parent #2 - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 Heterozygous PubMed: Auslender 2008 - - Germline - 5/582 controls - - - DNA SEQ - - USH2 - PubMed: Auslender 2008 Proband M - Uzbekistan - - - - - 1 Anne-Françoise Roux
+/+ 2 c.236_239dup r.(?) p.(Thr80Serfs*29) - Parent #2 - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 Heterozygous PubMed: Auslender 2008 - - Germline - 5/582 controls - - - DNA SEQ - - USH2 - PubMed: Auslender 2008 Relative M - Yemen - - - - - 1 Anne-Françoise Roux
+/+ 2 c.236_239dup r.(?) p.(Thr80Serfs*29) - Parent #1 - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 Heterozygous PubMed: Kaiserman 2007 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Kaiserman 2007 Proband F - Uzbekistan - - - - - 1 Anne-Françoise Roux
+/+ 2 c.236_239dup r.(?) p.(Thr80Serfs*29) - Paternal (inferred) - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 Homozygous PubMed: Auslender 2008 - - Germline - 5/582 controls - - - DNA SEQ - - USH2 - PubMed: Auslender 2008 Proband F - Iraq - - - - - 1 Anne-Françoise Roux
+/+ 2 c.236_239dup r.(?) p.(Thr80Serfs*29) - Maternal (inferred) - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 Homozygous PubMed: Auslender 2008 - - Germline - 5/582 controls - - - DNA SEQ - - USH2 - PubMed: Auslender 2008 Proband F - Iraq - - - - - 1 Anne-Françoise Roux
+/+ 2 c.236_239dup r.(?) p.(Thr80Serfs*29) - Parent #1 - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 Heterozygous PubMed: Najera 2002 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Najera 2002 Proband M - Spain - - - - - 1 Jose Maria Millan
+/+ 2 c.236_239dup r.(?) p.(Thr80Serfs*29) - Parent #1 - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 Heterozygous PubMed: Aller 2006 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Aller 2006 Relative F - Spain - - - - - 1 Jose Maria Millan
+/+ 2 c.236_239dup r.(?) p.(Thr80Serfs*29) - Parent #1 - pathogenic g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 Heterozygous PubMed: Aller 2006 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Aller 2006 Relative F - Spain - - - - - 1 Jose Maria Millan
+/. - c.236_239dup r.(?) p.(Gln81Tyrfs*28) - Unknown ACMG pathogenic g.216595440_216595443dup - - - USH2A_000135 - PubMed: Sharon 2019 - - Germline - 2/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 2 IRD families - - Israel - - - - - 2 Global Variome, with Curator vacancy
+/. - c.236_239dup r.(?) p.(Gln81Tyrfs*28) - Unknown ACMG pathogenic g.216595440_216595443dup - - - USH2A_000135 - PubMed: Sharon 2019 - - Germline - 17/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 17 IRD families - - Israel - - - - - 17 Global Variome, with Curator vacancy
+/. 2 c.236_239dup r.(?) p.(Gln81Tyrfs*28) - Both (homozygous) ACMG pathogenic (recessive) g.216595440_216595443dup - - - USH2A_000135 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH2A Pat20 PubMed: Bahena 2021 - F yes Iran - - - - - 2 Barbara Vona
+/. 2 c.236_239dup r.(?) p.(Gln81Tyrfs*28) - Both (homozygous) ACMG pathogenic (recessive) g.216595440_216595443dup g.216422098_216422101dup - - USH2A_000135 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH Pat58 PubMed: Bahena 2021 - M yes Iran - - - - - 1 Barbara Vona
?/. 2 c.236_239dup r.(?) p.(Gln81Tyrfs*28) - Unknown - VUS g.216595440_216595443dup - c.236_239dup - USH2A_000135 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA PCR, SEQ blood - retinal disease - PubMed: Khalaileh-2018 - F yes - Oriental Jew - - - - 1 LOVD
?/. 2 c.236_239dup r.(?) p.(Gln81Tyrfs*28) - Unknown - VUS g.216595440_216595443dup - c.236_239dup - USH2A_000135 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA SEQ-NG blood WES retinal disease - PubMed: Khalaileh-2018 - - yes - Jewish-Yemenite - - - - 1 LOVD
+/. - c.236_239dup r.(?) p.(Gln81TyrfsTer28) - Unknown ACMG pathogenic g.216595440_216595443dup g.216422098_216422101dup 236_239dupGTAC - USH2A_000135 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PP1_S PubMed: Aller, E. et al., 2006; PubMed: Bahena, P. et al., 2022; PubMed: Khalaileh, A. et al., 2018 - rs1553258097 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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