Variant #0000514577 (NC_000002.11:g.219209686_219209691del, NM_001077399.2:c.*72201_*72206del (PNKD))
| Chromosome |
2 |
| 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.219209686_219209691del |
| DNA change (hg38) |
g.218344963_218344968del |
| Published as |
PNKD(NM_015488.4):c.1140_1145delTATGCA (p.M381_H382del), PNKD(NM_015488.5):c.1140_1145delTATGCA (p.M381_H382del) |
| ISCN |
- |
| DB-ID |
PNKD_000013 See all 3 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 |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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