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) |

Variant on transcripts
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