Variant #0000623858 (NC_000018.9:g.46860094A>C, NC_000018.9(NM_017653.3):c.620+4T>G (DYM))
Chromosome |
18 |
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.46860094A>C |
DNA change (hg38) |
g.49333724A>C |
Published as |
DYM(NM_001353214.1):c.620+4T>G |
ISCN |
- |
DB-ID |
DYM_000015 |
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) |
0.00157 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-12-06 12:43:26 +01:00 (CET) |
Date last edited |
2020-07-14 18:50:07 +02:00 (CEST) |

Variant on transcripts
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