Variant #0000859566 (NC_000004.11:g.661663G>A, NM_000283.3:c.2371G>A (PDE6B))

Chromosome 4
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.661663G>A
DNA change (hg38) -
Published as PDE6B(NM_000283.3):c.2371G>A (p.E791K)
ISCN -
DB-ID ATP5I_000003
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) 0.00035 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE6B NM_000283.3 -?/. - c.2371G>A r.(?) p.(Glu791Lys)
ATP5I NM_007100.3 -?/. - c.*4626C>T r.(=) p.(=)


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