Variant #0000924846 (NC_000008.10:g.145738425_145738430dup, NM_004260.3:c.2569_2574dup (RECQL4))
Chromosome |
8 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.145738425_145738430dup |
DNA change (hg38) |
- |
Published as |
RECQL4(NM_004260.3):c.2569_2574dupTGCACC (p.C857_T858dup), RECQL4(NM_004260.3):c.2575_2576insTGCACC (p.(Cys857_Thr858dup)), RECQL4(NM_004260.4):c.2... |
ISCN |
- |
DB-ID |
RECQL4_000030 See all 3 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_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2023-04-16 21:50:28 +02:00 (CEST) |
Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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