Variant #0000306908 (NC_000008.10:g.145741503C>A, NM_004260.3:c.1000G>T (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.145741503C>A
DNA change (hg38) g.144516119C>A
Published as RECQL4(NM_004260.3):c.1000G>T (p.E334*)
ISCN -
DB-ID RECQL4_000050 See all 2 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-25 11:36:37 +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.*6356G>T r.(=) p.(=)
RECQL4 NM_004260.3 +/. - c.1000G>T r.(?) p.(Glu334Ter)
LRRC14 NM_014665.3 +/. - c.-2034C>A r.(?) p.(=)
MFSD3 NM_138431.1 +/. - c.*4956C>A r.(=) p.(=)


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