Variant #0000953598 (NC_000001.10:g.215812574_215812575del, NM_206933.2:c.14977_14978del (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.215812574_215812575del
DNA change (hg38) g.215639232_215639233del
Published as 14977_14978delTT
ISCN -
DB-ID USH2A_000272 See all 15 reported entries
Variant remarks ACMG GN005 criteria: PVS1_VS PM2_P PM3_M
Reference PubMed: Bonnet, C. et al., 2016; PubMed: Colombo, L. et al., 2022; PubMed: Colombo, L. et al., 2022; PubMed: Karali, M. et al., 2019; PubMed: Colombo, L. et al., 2021; PubMed: Eandi, C. M. et al., 2017
ClinVar ID -
dbSNP ID rs747160949
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 2023-12-12 17:06:01 +01:00 (CET)
Date last edited 2023-12-13 17:38:50 +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 +/. - c.14977_14978del r.(?) p.(Phe4993ProfsTer7) -


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