Variant #0000529896 (NC_000006.11:g.80203325C>G, NC_000006.11(NM_181714.3):c.858+5G>C (LCA5))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.80203325C>G
DNA change (hg38) g.79493608C>G
Published as LCA5(NM_181714.3):c.858+5G>C
ISCN -
DB-ID LCA5_000061
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LCA5 NM_001122769.2 -?/. - c.858+5G>C r.spl? p.?
LCA5 NM_181714.3 -?/. - c.858+5G>C r.spl? p.?


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