Variant #0000349071 (NC_000001.10:g.215799170T>C, NM_206933.2:c.15562A>G (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.215799170T>C
DNA change (hg38) g.215625828T>C
Published as USH2A(NM_206933.2):c.15562A>G (p.(Ser5188Gly))
ISCN -
DB-ID USH2A_000281 See all 15 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01269 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
KCTD3 NM_016121.3 -/. - c.*5210T>C r.(=) p.(=) -
USH2A NM_206933.2 -/. - c.15562A>G r.(?) p.(Ser5188Gly) -


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