Variant #0000953456 (NC_000001.10:g.215848243G>A, NM_206933.2:c.13010C>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.215848243G>A
DNA change (hg38) g.215674901G>A
Published as -
ISCN -
DB-ID USH2A_000194 See all 48 reported entries
Variant remarks ACMG GN005 criteria: PM2_P PM3_VS PP1_P
Reference PubMed: Lenassi, E. et al., 2015; PubMed: Reurink, J. et al., 2021; PubMed: Meng, X. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Perez-Carro, R. et al., 2018; PubMed: Aller, E. et al., 2006; PubMed: Mansard, L. et al., 2021; PubMed: Weisschuh, N. et al., 2020; PubMed: Jauregui, R. et al., 2020; PubMed: Inaba, A. et al., 2020; PubMed: Huang, X. F. et al., 2015; PubMed: Neuhaus, C. et al., 2017
ClinVar ID -
dbSNP ID rs527236137
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner David Baux
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by David Baux
Date created 2023-12-12 17:03:19 +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.13010C>T r.(?) p.(Thr4337Met) -


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