Variant #0000611540 (NC_000008.10:g.145738767del, NM_004260.3:c.2299del (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.145738767del
DNA change (hg38) g.144513384del
Published as RECQL4(NM_004260.3):c.2300del (p.(Gly767ValfsTer443))
ISCN -
DB-ID RECQL4_000221
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +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.*9094del r.(?) p.(=)
RECQL4 NM_004260.3 ?/. - c.2299del r.(?) p.(Val767TrpfsTer76)
LRRC14 NM_014665.3 ?/. - c.-4770del r.(?) p.(=)
MFSD3 NM_138431.1 ?/. - c.*2220del r.(?) p.(=)


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