Variant #0000953095 (NC_000001.10:g.216138711A>C, NM_206933.2:c.7068T>G (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.216138711A>C
DNA change (hg38) g.215965369A>C
Published as -
ISCN -
DB-ID USH2A_000779 See all 26 reported entries
Variant remarks ACMG GN005 criteria: PP1_P PM3_P BS1_P
Reference PubMed: Gao, F. J. et al., 2021; PubMed: Sun, T. et al., 2018; PubMed: Ma, D. J. et al., 2021; PubMed: Meng, X. et al., 2021; PubMed: Maltese, P. E. et al., 2022; PubMed: Inaba, A. et al., 2020; PubMed: Huang, X. F. et al., 2015
ClinVar ID -
dbSNP ID rs200038092
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00078 View details
Owner David Baux
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by David Baux
Date created 2023-12-12 16:58:34 +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.7068T>G r.(?) p.(Asn2356Lys) -


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