Variant #0001052088 (NC_000005.9:g.127800487C>A, NM_001999.3:c.756G>T (FBN2))
| Chromosome |
5 |
| 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.127800487C>A |
| DNA change (hg38) |
- |
| Published as |
FBN2(NM_001999.3):c.756G>T (p.E252D), FBN2(NM_001999.4):c.756G>T (p.(Glu252Asp)) |
| ISCN |
- |
| DB-ID |
FBN2_000137 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 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2025-11-01 13:22:20 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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