Variant #0000016808 (NC_000008.10:g.145738796G>A, NM_004260.3:c.2269C>T (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.145738796G>A |
| DNA change (hg38) |
g.144513412G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
RECQL4_000002 See all 7 reported entries |
| Variant remarks |
1 Finnish family (com-het) with RAPADILINO syndrome |
| Reference |
PubMed: Siitonen et al. 2009 |
| ClinVar ID |
- |
| dbSNP ID |
rs137853229 |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00012 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| 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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