Variant #0000924846 (NC_000008.10:g.145738425_145738430dup, NM_004260.3:c.2569_2574dup (RECQL4))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.145738425_145738430dup
DNA change (hg38) -
Published as RECQL4(NM_004260.3):c.2569_2574dupTGCACC (p.C857_T858dup), RECQL4(NM_004260.3):c.2575_2576insTGCACC (p.(Cys857_Thr858dup)), RECQL4(NM_004260.4):c.2...
ISCN -
DB-ID RECQL4_000030 See all 3 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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC24 NM_001024678.3 -?/. - c.*9443_*9448dup r.(=) p.(=)
RECQL4 NM_004260.3 -?/. - c.2569_2574dup r.(?) p.(Cys857_Thr858dup)
LRRC14 NM_014665.3 -?/. - c.-5112_-5107dup r.(?) p.(=)
MFSD3 NM_138431.1 -?/. - c.*1878_*1883dup r.(=) p.(=)


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