Variant #0000656054 (NC_000008.10:g.145741169C>T, NM_004260.3:c.1237G>A (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.145741169C>T |
DNA change (hg38) |
g.144515785C>T |
Published as |
RECQL4(NM_004260.3):c.1237G>A (p.A413T, p.(Ala413Thr)) |
ISCN |
- |
DB-ID |
RECQL4_000117 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) |
0.00091 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2020-06-25 11:33:06 +02:00 (CEST) |

Variant on transcripts
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