Variant #0000953048 (NC_000001.10:g.216172258G>C, NM_206933.2:c.6628C>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.216172258G>C
DNA change (hg38) g.215998916G>C
Published as -
ISCN -
DB-ID USH2A_001221 See all 12 reported entries
Variant remarks ACMG GN005 criteria:
Reference PubMed: Qu, L. H. et al., 2020; PubMed: Sun, T. et al., 2018
ClinVar ID -
dbSNP ID rs192115090
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00077 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.6628C>G r.(?) p.(Pro2210Ala) -


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