Variant #0000543971 (NC_000011.9:g.45955752T>C, NM_001101802.1:c.1810A>G (PHF21A))
| Chromosome |
11 |
| 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.45955752T>C |
| DNA change (hg38) |
g.45934201T>C |
| Published as |
PHF21A(NM_001101802.1):c.1810A>G (p.I604V), PHF21A(NM_001101802.3):c.1810A>G (p.I604V) |
| ISCN |
- |
| DB-ID |
PHF21A_000001 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) |
0.00144 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
|