Variant #0000311180 (NC_000001.10:g.216420437del, NM_206933.2:c.2299del (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.216420437del
DNA change (hg38) g.216247095del
Published as USH2A(NM_007123.5):c.2299del (p.(Glu767SerfsTer21)), USH2A(NM_206933.2):c.2299delG (p.E767Sfs*21), USH2A(NM_206933.4):c.2299delG (p.E767Sfs*21)
ISCN -
DB-ID USH2A_000001 See all 1071 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00074 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +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 +/. - c.2299del r.(?) p.(Glu767SerfsTer21) -


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