Variant #0000538386 (NC_000009.11:g.70176769del, NM_001126334.1:c.1215del (FOXD4L5))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.70176769del
DNA change (hg38) g.65283163del
Published as FOXD4L5(NM_001126334.1):c.1215delC (p.W406Gfs*21)
ISCN -
DB-ID FOXD4L5_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) 0.00391 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-25 14:04:54 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FOXD4L5 NM_001126334.1 -/. - c.1215del r.(?) p.(Trp406GlyfsTer21)


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