Variant #0000717139 (NC_000001.10:g.215799182T>G, NM_206933.2:c.15550A>C (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.215799182T>G
DNA change (hg38) -
Published as USH2A(NM_206933.2):c.15550A>C (p.I5184L)
ISCN -
DB-ID USH2A_001834
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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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.*5222T>G r.(=) p.(=) -
USH2A NM_206933.2 ?/. - c.15550A>C r.(?) p.(Ile5184Leu) -


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