Variant #0000343363 (NC_000004.11:g.661655G>A, NM_000283.3:c.2363G>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.661655G>A
DNA change (hg38) g.667866G>A
Published as PDE6B(NM_000283.3):c.2363G>A (p.R788H)
ISCN -
DB-ID PDE6B_000064 See all 4 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) 0.0001 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 2019-12-04 14:54:23 +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.2363G>A r.(?) p.(Arg788His)
ATP5I NM_007100.3 ?/. - c.*4634C>T r.(=) p.(=)


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