Variant #0000287538 (NC_000019.9:g.47259163C>G, NM_024301.4:c.456C>G (FKRP))
| Chromosome |
19 |
| 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.47259163C>G |
| DNA change (hg38) |
g.46755906C>G |
| Published as |
FKRP(NM_001039885.2):c.456C>G (p.S152R, p.(Ser152Arg)), FKRP(NM_001039885.3):c.456C>G (p.S152R), FKRP(NM_024301.5):c.456C>G (p.S152R) |
| ISCN |
- |
| DB-ID |
FKRP_000095 See all 9 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) |
0.00049 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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