Variant #0000287259 (NC_000015.9:g.48717607G>C, NM_000138.4:c.7412C>G (FBN1))
Chromosome |
15 |
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.48717607G>C |
DNA change (hg38) |
g.48425410G>C |
Published as |
FBN1(NM_000138.4):c.7412C>G (p.P2471R, p.(Pro2471Arg)), FBN1(NM_000138.5):c.7412C>G (p.P2471R) |
ISCN |
- |
DB-ID |
FBN1_000099 See all 6 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) |
2.0E-5 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 |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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