Variant #0000278756 (NC_000006.11:g.80197069G>A, NM_181714.3:c.1746C>T (LCA5))

Chromosome 6
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.80197069G>A
DNA change (hg38) g.79487352G>A
Published as LCA5(NM_181714.4):c.1746C>T (p.N582=)
ISCN -
DB-ID LCA5_000045
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) 0.00019 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.1746C>T r.(?) p.(Asn582=)
LCA5 NM_181714.3 -/. - c.1746C>T r.(?) p.(Asn582=)


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