Variant #0000524800 (NC_000005.9:g.149323933G>T, NM_000440.2:c.304C>A (PDE6A))

Chromosome 5
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.149323933G>T
DNA change (hg38) g.149944370G>T
Published as PDE6A(NM_000440.2):c.304C>A (p.R102S), PDE6A(NM_000440.3):c.304C>A (p.R102S)
ISCN -
DB-ID PDE6A_000048 See all 52 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) 0.00016 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE6A NM_000440.2 +?/. - c.304C>A r.(?) p.(Arg102Ser)


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