Variant #0000921503 (NC_000001.10:g.215990476G>A, NM_206933.2:c.9433C>T (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.215990476G>A
DNA change (hg38) g.215817134G>A
Published as -
ISCN -
DB-ID USH2A_001187 See all 16 reported entries
Variant remarks PM2_P, PM3_S following ClinGen GN005
Reference -
ClinVar ID -
dbSNP ID rs267598373
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 2023-03-17 17:42:01 +01:00 (CET)
Date last edited 2023-03-17 17:43:36 +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 ?/? 48 c.9433C>T r.(?) p.(Leu3145Phe) Fibronectin type-III 18 (3113 - 3209)


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