Variant #0000528886 (NC_000006.11:g.42975009G>A, NM_006245.3:c.598G>A (PPP2R5D))
| Chromosome |
6 |
| 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.42975009G>A |
| DNA change (hg38) |
g.43007271G>A |
| Published as |
PPP2R5D(NM_001270476.1):c.145G>A (p.E49K, p.(Glu49Lys)), PPP2R5D(NM_001270476.2):c.145G>A (p.E49K) |
| ISCN |
- |
| DB-ID |
MEA1_000003 See all 11 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) |
Retrieve |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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