Variant #0000692638 (NC_000019.9:g.10283803C>T, NM_001379.2:c.683G>A (DNMT1))
Chromosome |
19 |
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.10283803C>T |
DNA change (hg38) |
- |
Published as |
DNMT1(NM_001130823.1):c.731G>A (p.(Gly244Glu)), DNMT1(NM_001130823.3):c.731G>A (p.G244E), DNMT1(NM_001379.3):c.683G>A (p.G228E) |
ISCN |
- |
DB-ID |
DNMT1_000044 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) |
0.00111 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2020-09-15 15:50:26 +02:00 (CEST) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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