Variant #0000693536 (NC_000023.10:g.24382417_24382428del, NM_001136234.1:c.1540_1551del (SUPT20HL1))
| Chromosome |
X |
| 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.24382417_24382428del |
| DNA change (hg38) |
- |
| Published as |
SUPT20HL1(NM_001136234.1):c.1497_1508del (p.(Ala504_Ala507del)), SUPT20HL1(NM_001136234.2):c.1618_1629delGCTGCTGCTGCT (p.A540_A543del) |
| ISCN |
- |
| DB-ID |
SUPT20HL1_000017 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) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2020-09-15 15:50:26 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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