Variant #0000342474 (NC_000004.11:g.647723G>A, NM_000283.3:c.794G>A (PDE6B))

Chromosome 4
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.647723G>A
DNA change (hg38) g.653934G>A
Published as PDE6B(NM_000283.3):c.794G>A (p.R265Q), PDE6B(NM_000283.4):c.794G>A (p.R265Q)
ISCN -
DB-ID PDE6B_000034 See all 7 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) 0.00109 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE6B NM_000283.3 ?/. - c.794G>A r.(?) p.(Arg265Gln)


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