Variant #0000952669 (NC_000001.10:g.216498883G>T, NM_206933.2:c.907C>A (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.216498883G>T
DNA change (hg38) g.216325541G>T
Published as -
ISCN -
DB-ID USH2A_000189 See all 11 reported entries
Variant remarks ACMG GN005 criteria: PM2_P PM3_M PP1_S
Reference PubMed: Gonzalez-Del Pozo, M. et al., 2018
ClinVar ID -
dbSNP ID rs748465849
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-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.907C>A r.(?) p.(Arg303Ser) -


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