Variant #0000016799 (NC_000008.10:g.145741697C>T, NM_004260.3:c.806G>A (RECQL4))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.145741697C>T
DNA change (hg38) g.144516313C>T
Published as c.806G>A (W269X); RAPADILINO 2
ISCN -
DB-ID RECQL4_000010
Variant remarks 1 Finnish family (com-het) with RAPADILINO syndrome
Reference PubMed: Siitonen et al. 2003
ClinVar ID -
dbSNP ID rs137853231
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Anne Polvi
Database submission license No license selected
Created by Anne Polvi
Date created 2012-12-10 17:19:31 +01:00 (CET)
Date last edited 2017-05-05 19:04:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RECQL4 NM_004260.3 +?/+? 05 c.806G>A r.(806g>a) p.(Trp269*)


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