Variant #0000953337 (NC_000001.10:g.215933077C>T, NM_206933.2:c.11156G>A (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.215933077C>T
DNA change (hg38) g.215759735C>T
Published as -
ISCN -
DB-ID USH2A_000433 See all 75 reported entries
Variant remarks ACMG GN005 criteria: PM2_P PM3_VS PP1_S
Reference PubMed: Gao, F. J. et al., 2021; PubMed: Lenassi, E. et al., 2015; PubMed: Sun, T. et al., 2018; PubMed: Ma, D. J. et al., 2021; PubMed: Meng, X. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Dan, H. et al., 2020; PubMed: Huang, L. et al., 2018; PubMed: Fu, Y. C. et al., 2018; PubMed: Gonzalez-Del Pozo, M. et al., 2018; PubMed: Chen, X. et al., 2014; PubMed: Kim, Y. N. et al., 2021; PubMed: Sun, Y. et al., 2020; PubMed: Weisschuh, N. et al., 2020; PubMed: Inaba, A. et al., 2020; PubMed: Bravo-Gil, N. et al., 2017
ClinVar ID -
dbSNP ID rs527236139
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 5.0E-5 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 17:01:57 +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.11156G>A r.(?) p.(Arg3719His) -


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