Variant #0001036886 (NC_000008.10:g.145741604C>A, NM_004260.3:c.899G>T (RECQL4))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.145741604C>A
DNA change (hg38) -
Published as RECQL4(NM_004260.4):c.899G>T (p.(Gly300Val))
ISCN -
DB-ID RECQL4_000338
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC24 NM_001024678.3 ?/. - c.*6255G>T r.(=) p.(=)
RECQL4 NM_004260.3 ?/. - c.899G>T r.(?) p.?
LRRC14 NM_014665.3 ?/. - c.-1933C>A r.(?) p.(=)
MFSD3 NM_138431.1 ?/. - c.*5057C>A r.(=) p.(=)


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