Variant #0000576683 (NC_000023.10:g.53966879C>T, NM_015107.2:c.2720G>A (PHF8))
| Chromosome |
X |
| 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.53966879C>T |
| DNA change (hg38) |
g.53940446C>T |
| Published as |
PHF8(NM_001184896.1):c.2828G>A (p.(Arg943His)), PHF8(NM_015107.2):c.2720G>A (p.R907H), PHF8(NM_015107.3):c.2720G>A (p.R907H) |
| ISCN |
- |
| DB-ID |
PHF8_000012 See all 4 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) |
0.00213 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| 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
|