Variant #0000931689 (NC_000001.10:g.215955488C>T, NM_206933.2:c.10636G>A (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.215955488C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID USH2A_000290 See all 15 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1553261372
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-08-03 11:46:01 +02:00 (CEST)
Date last edited N/A
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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.10636G>A r.(?) p.(Gly3546Arg) -


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