Variant #0000803555 (NC_000008.10:g.145738439_145738440del, NM_004260.3:c.2547_2548del (RECQL4))

Chromosome 8
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.145738439_145738440del
DNA change (hg38) -
Published as RECQL4(NM_004260.3):c.2547_2548delGT (p.F850Pfs*33)
ISCN -
DB-ID RECQL4_000246 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
LRRC24 NM_001024678.3 +/. - c.*9421_*9422del r.(=) p.(=)
RECQL4 NM_004260.3 +/. - c.2547_2548del r.(?) p.(Phe850Profs*33)
LRRC14 NM_014665.3 +/. - c.-5098_-5097del r.(?) p.(=)
MFSD3 NM_138431.1 +/. - c.*1892_*1893del r.(=) p.(=)


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