Variant #0000611631 (NC_000008.10:g.48777112G>A, NC_000008.10(NM_006904.6):c.5571+5C>T (PRKDC))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48777112G>A |
| DNA change (hg38) |
g.47864551G>A |
| Published as |
PRKDC(NM_006904.6):c.5571+5C>T |
| ISCN |
- |
| DB-ID |
PRKDC_000070 |
| 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) |
0.00013 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2020-06-23 19:43:30 +02:00 (CEST) |

Variant on transcripts
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