Variant #0000569374 (NC_000020.10:g.31387951C>T, NC_000020.10(NM_006892.3):c.1760-8C>T (DNMT3B))
Chromosome |
20 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.31387951C>T |
DNA change (hg38) |
g.32800145C>T |
Published as |
DNMT3B(NM_001207055.1):c.1574-8C>T (p.(=)), DNMT3B(NM_006892.3):c.1760-8C>T |
ISCN |
- |
DB-ID |
DNMT3B_000052 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) |
0.00515 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2019-12-04 15:24:38 +01:00 (CET) |

Variant on transcripts
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