Variant #0000931184 (NC_000020.10:g.5282850C>T, NM_144773.2:c.991G>A (PROKR2))
| Chromosome |
20 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5282850C>T |
| DNA change (hg38) |
- |
| Published as |
PROKR2(NM_144773.3):c.991G>A (p.V331M), PROKR2(NM_144773.4):c.991G>A (p.V331M) |
| ISCN |
- |
| DB-ID |
PROKR2_000018 See all 2 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) |
0.00621 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2023-07-07 10:10:56 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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