Variant #0000880275 (NC_000001.10:g.215848408A>G, NM_206933.2:c.12845T>C (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.215848408A>G
DNA change (hg38) g.215675066A>G
Published as -
ISCN -
DB-ID USH2A_000315 See all 10 reported entries
Variant remarks PM2_Sup PM3_St PP1_Sup following GN005
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner David Baux
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by David Baux
Date created 2022-10-05 10:18:01 +02:00 (CEST)
Date last edited 2022-10-05 10:28:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
USH2A NM_206933.2 +?/+? 63 c.12845T>C r.(?) p.(Leu4282Pro) Fibronectin type-III 28 (4262 - 4357)


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