Variant #0000952757 (NC_000001.10:g.216462717G>A, NM_206933.2:c.1876C>T (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.216462717G>A
DNA change (hg38) g.216289375G>A
Published as -
ISCN -
DB-ID USH2A_000010 See all 58 reported entries
Variant remarks ACMG GN005 criteria: PVS1_VS PM2_P PM3_VS
Reference PubMed: Lenassi, E. et al., 2015; PubMed: Sun, T. et al., 2018; PubMed: Bonnet, C. et al., 2016; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Jiang, L. et al., 2015; PubMed: Colombo, L. et al., 2022; PubMed: Wafa, T. T. et al., 2021; PubMed: Toms, M. et al., 2020; PubMed: Mansard, L. et al., 2021; PubMed: Weisschuh, N. et al., 2020; PubMed: Colombo, L. et al., 2021; PubMed: Neuhaus, C. et al., 2017
ClinVar ID -
dbSNP ID rs534534437
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-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 16:51:47 +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.1876C>T r.(?) p.(Arg626Ter) -


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