Variant #0000789171 (NC_000001.10:g.215847604A>C, NM_206933.2:c.13649T>G (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.215847604A>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID USH2A_001895 See all 6 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs553956503
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00033 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-06-15 11:43:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +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 +?/. - c.13649T>G r.(?) p.(Val4550Gly) -


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