Variant #0000619299 (NC_000023.10:g.153599528_153599529insTA, NM_001110556.1:c.85_86insTA (FLNA))
| 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.153599528_153599529insTA |
| DNA change (hg38) |
g.154371160_154371161insTA |
| Published as |
FLNA(NM_001110556.1):c.85_86insTA (p.(Pro29LeufsTer30)) |
| ISCN |
- |
| DB-ID |
FLNA_000430 |
| 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 |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2020-07-21 16:31:12 +02:00 (CEST) |

Variant on transcripts
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