Variant #0000522785 (NC_000004.11:g.619540_619541insTGCGA, NM_000283.3:c.125_126insTGCGA (PDE6B))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.619540_619541insTGCGA
DNA change (hg38) g.625751_625752insTGCGA
Published as PDE6B(NM_000283.3):c.125_126insTGCGA (p.D43Afs*109)
ISCN -
DB-ID PDE6B_000120
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 10:23:43 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE6B NM_000283.3 +/. - c.125_126insTGCGA r.(?) p.(Asp43AlafsTer109)


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