Variant #0000538983 (NC_000010.10:g.104590549_104590552dup, NM_000102.3:c.1435_1438dup (CYP17A1))
| Chromosome |
10 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.104590549_104590552dup |
| DNA change (hg38) |
g.102830792_102830795dup |
| Published as |
CYP17A1(NM_000102.3):c.1435_1438dupATCC (p.P480Hfs*27), CYP17A1(NM_000102.4):c.1435_1438dupATCC (p.P480Hfs*27) |
| ISCN |
- |
| DB-ID |
CYP17A1_000010 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) |
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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