Variant #0000917027 (NC_000001.10:g.216270451G>A, NM_206933.2:c.4732C>T (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.216270451G>A
DNA change (hg38) g.216097109G>A
Published as -
ISCN -
DB-ID USH2A_000528 See all 19 reported entries
Variant remarks PM2_S, PM3_VS, PP3_S (following ClinGen GN005)
Reference -
ClinVar ID -
dbSNP ID rs201529124
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 2023-01-17 17:35:01 +01:00 (CET)
Date last edited 2023-01-17 17:36:30 +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 +?/+? 22 c.4732C>T r.(?) p.(Arg1578Cys) -


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