Variant #0001027462 (NC_000023.10:g.153599552_153599554dup, NM_001110556.1:c.62_64dup (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.153599552_153599554dup |
DNA change (hg38) |
- |
Published as |
FLNA(NM_001110556.1):c.64_65insTCG (p.(Val21dup)), FLNA(NM_001110556.2):c.58_60dupTCG (p.V21dup), FLNA(NM_001110556.2):c.62_64dupTCG (p.V21dup) |
ISCN |
- |
DB-ID |
FLNA_000281 See all 5 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 |
2025-02-07 18:57:27 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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