Variant #0000880276 (NC_000001.10:g.215955412G>A, NM_206933.2:c.10712C>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.215955412G>A
DNA change (hg38) g.215782070G>A
Published as -
ISCN -
DB-ID USH2A_000115 See all 70 reported entries
Variant remarks PM2_Sup PM3_St PP1_M PP4_Sup following GN005
Reference -
ClinVar ID ClinVar-48355
dbSNP ID rs202175091
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 2022-10-05 10:34:01 +02:00 (CEST)
Date last edited 2022-10-05 10:36:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
USH2A NM_206933.2 +?/+? 54 c.10712C>T r.(?) p.(Thr3571Met) Fibronectin type-III 20 (3501 - 3589)


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