Variant #0000917028 (NC_000001.10:g.215848360T>C, NM_206933.2:c.12893A>G (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.215848360T>C
DNA change (hg38) g.215675018T>C
Published as -
ISCN -
DB-ID USH2A_001042 See all 3 reported entries
Variant remarks PM2_S, PM3_M, PP3_S (following ClinGen GN005)
Reference -
ClinVar ID -
dbSNP ID -
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 2023-01-17 17:38:01 +01:00 (CET)
Date last edited 2023-01-17 17:41:12 +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 ?/? 63 c.12893A>G r.(?) p.(Tyr4298Cys) -


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