Variant #0000334013 (NC_000023.10:g.48681883C>T, NM_006044.2:c.3074C>T (HDAC6))
| 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.48681883C>T |
| DNA change (hg38) |
g.48823473C>T |
| Published as |
HDAC6(NM_001321226.1):c.3074C>T (p.S1025L), HDAC6(NM_006044.2):c.3074C>T (p.(Ser1025Leu)), HDAC6(NM_006044.3):c.3074C>T (p.S1025L) |
| ISCN |
- |
| DB-ID |
HDAC6_000026 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) |
0.00186 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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