Variant #0000656045 (NC_000008.10:g.145738492_145738493del, NM_004260.3:c.2492_2493del (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.145738492_145738493del
DNA change (hg38) g.144513109_144513110del
Published as RECQL4(NM_004260.3):c.2492_2493delAT (p.H831Rfs*52), RECQL4(NM_004260.4):c.2492_2493del (p.(His831Argfs*52))
ISCN -
DB-ID RECQL4_000003 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) 8.0E-5 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC24 NM_001024678.3 +/. - c.*9366_*9367del r.(=) p.(=)
RECQL4 NM_004260.3 +/. - c.2492_2493del r.(?) p.(His831ArgfsTer52)
LRRC14 NM_014665.3 +/. - c.-5045_-5044del r.(?) p.(=)
MFSD3 NM_138431.1 +/. - c.*1945_*1946del r.(=) p.(=)


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