Variant #0000912919 (NC_000008.10:g.145741454_145741455del, NM_004260.3:c.1048_1049del (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.145741454_145741455del
DNA change (hg38) -
Published as RECQL4(NM_004260.3):c.1048_1049del (p.(Arg350Glyfs*21)), RECQL4(NM_004260.4):c.1048_1049delAG (p.R350Gfs*21)
ISCN -
DB-ID RECQL4_000140 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.*6404_*6405del r.(=) p.(=)
RECQL4 NM_004260.3 +/. - c.1048_1049del r.(?) p.(Arg350GlyfsTer21)
LRRC14 NM_014665.3 +/. - c.-2083_-2082del r.(?) p.(=)
MFSD3 NM_138431.1 +/. - c.*4907_*4908del r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.