Variant #0000692417 (NC_000017.10:g.58740482_58740483insTA, NM_003620.3:c.1387_1388insTA (PPM1D))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.58740482_58740483insTA |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
PPM1D_000018 |
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_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2020-09-15 15:50:26 +02:00 (CEST) |
Date last edited |
2021-02-08 18:36:18 +01:00 (CET) |

Variant on transcripts
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