Variant #0000655316 (NC_000005.9:g.146258293T>A, NC_000005.9(NM_181678.2):c.-48-22147A>T (PPP2R2B))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.146258293T>A |
DNA change (hg38) |
g.146878730T>A |
Published as |
PPP2R2B(NM_181675.3):c.55A>T (p.S19C) |
ISCN |
- |
DB-ID |
PPP2R2B_000020 |
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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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