Variant #0000952673 (NC_000001.10:g.216498841G>T, NM_206933.2:c.949C>A (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.216498841G>T
DNA change (hg38) g.216325499G>T
Published as -
ISCN -
DB-ID USH2A_000155 See all 50 reported entries
Variant remarks ACMG GN005 criteria: PS4_P PM2_P PM3_VS PP3_P PP1_P
Reference PubMed: Reurink, J. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Pennings, R. J. et al., 2004; PubMed: Wafa, T. T. et al., 2021; PubMed: Mansard, L. et al., 2021; PubMed: Panagiotou, E. S. et al., 2020; PubMed: Karali, M. et al., 2019; PubMed: Weisschuh, N. et al., 2020; PubMed: Neuhaus, C. et al., 2017
ClinVar ID -
dbSNP ID rs111033272
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner David Baux
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by David Baux
Date created 2023-12-12 16:50:20 +01:00 (CET)
Date last edited 2023-12-13 17:38:50 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
USH2A NM_206933.2 +/. - c.949C>A r.(949c>a,951_1143del) p.(=,Tyr318CysfsTer17) -


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