Variant #0000306914 (NC_000008.10:g.145739007G>C, NM_004260.3:c.2148C>G (RECQL4))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.145739007G>C |
| DNA change (hg38) |
g.144513623G>C |
| Published as |
RECQL4(NM_004260.3):c.2148C>G (p.I716M) |
| ISCN |
- |
| DB-ID |
RECQL4_000095 |
| 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) |
2.0E-5 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2020-06-25 11:19:10 +02:00 (CEST) |

Variant on transcripts
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