Variant #0000621025 (NC_000002.11:g.28999810C>G, NM_002709.2:c.146C>G (PPP1CB))
| Chromosome |
2 |
| 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.28999810C>G |
| DNA change (hg38) |
g.28776944C>G |
| Published as |
PPP1CB(NM_002709.2):c.146C>G (p.(Pro49Arg)), PPP1CB(NM_002709.3):c.146C>G (p.P49R), PPP1CB(NM_206876.2):c.146C>G (p.P49R) |
| ISCN |
- |
| DB-ID |
PPP1CB_000001 See all 4 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_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2019-12-06 12:43:26 +01:00 (CET) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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