Variant #0000953056 (NC_000001.10:g.216166454T>G, NM_206933.2:c.6713A>C (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.216166454T>G
DNA change (hg38) g.215993112T>G
Published as -
ISCN -
DB-ID USH2A_000062 See all 22 reported entries
Variant remarks ACMG GN005 criteria: BA1 BS2_S
Reference PubMed: Glockle, N. et al., 2014; PubMed: Colombo, L. et al., 2022; PubMed: Colombo, L. et al., 2021; PubMed: Colombo, L. et al., 2021
ClinVar ID -
dbSNP ID rs41277212
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.02247 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 16:57:43 +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.6713A>C r.(?) p.(Glu2238Ala) -


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