Variant #0000953008 (NC_000001.10:g.216243634G>C, NM_206933.2:c.5858C>G (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.216243634G>C
DNA change (hg38) g.216070292G>C
Published as -
ISCN -
DB-ID USH2A_000342 See all 20 reported entries
Variant remarks ACMG GN005 criteria: BS1_P BS2_S BP4_P
Reference PubMed: Colombo, L. et al., 2022; PubMed: Ganapathi, M. et al., 2022
ClinVar ID -
dbSNP ID rs41302239
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00081 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 16:57:01 +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.5858C>G r.(?) p.(Ala1953Gly) -


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