Variant #0001036885 (NC_000008.10:g.145741431T>C, NM_004260.3:c.1072A>G (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.145741431T>C
DNA change (hg38) -
Published as RECQL4(NM_004260.4):c.1072A>G (p.(Met358Val))
ISCN -
DB-ID RECQL4_000337
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) 4.0E-5 View details
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC24 NM_001024678.3 -?/. - c.*6428A>G r.(=) p.(=)
RECQL4 NM_004260.3 -?/. - c.1072A>G r.(?) p.?
LRRC14 NM_014665.3 -?/. - c.-2106T>C r.(?) p.(=)
MFSD3 NM_138431.1 -?/. - c.*4884T>C r.(=) p.(=)


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