Variant #0000554755 (NC_000015.9:g.51514572G>A, NM_000103.3:c.602C>T (CYP19A1))
| Chromosome |
15 |
| 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.51514572G>A |
| DNA change (hg38) |
g.51222375G>A |
| Published as |
CYP19A1(NM_000103.3):c.602C>T (p.(Thr201Met)), CYP19A1(NM_031226.3):c.602C>T (p.T201M) |
| ISCN |
- |
| DB-ID |
CYP19A1_000006 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) |
0.02371 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
|