Variant #0000808264 (NC_000017.10:g.74133995dup, NM_001454.3:c.709dup (FOXJ1))

Chromosome 17
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.74133995dup
DNA change (hg38) -
Published as FOXJ1(NM_001454.4):c.709dupC (p.R237Pfs*37)
ISCN -
DB-ID FOXJ1_000006
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +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     
FOXJ1 NM_001454.3 +/. - c.709dup r.(?) p.(Arg237Profs*37)
RNF157 NM_052916.2 +/. - c.*7325dup r.(?) p.(=)


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