Variant #0000998763 (NC_000011.9:g.118342866G>C, NM_001197104.1:c.992G>C (KMT2A))
| Chromosome |
11 |
| 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.118342866G>C |
| DNA change (hg38) |
- |
| Published as |
KMT2A(NM_001197104.1):c.992G>C (p.(Arg331Pro)) |
| ISCN |
- |
| DB-ID |
KMT2A_000344 |
| 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_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2024-08-28 13:16:32 +02:00 (CEST) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
|