Variant #0000253535 (NC_000013.10:g.28608241A>G, NM_004119.2:c.1815T>C (FLT3))
| Chromosome |
13 |
| 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.28608241A>G |
| DNA change (hg38) |
g.28034104A>G |
| Published as |
FLT3(NM_004119.2):c.1815T>C (p.F605=) |
| ISCN |
- |
| DB-ID |
FLT3_000001 |
| 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) |
0.00131 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2020-07-03 14:36:50 +02:00 (CEST) |

Variant on transcripts
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