Variant #0000960370 (NC_000001.10:g.11087637A>G, NM_007375.3:c.*4926A>G (TARDBP))
Chromosome |
1 |
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.11087637A>G |
DNA change (hg38) |
- |
Published as |
MASP2(NM_006610.4):c.1366T>C (p.F456L) |
ISCN |
- |
DB-ID |
MASP2_000035 |
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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2024-02-26 20:06:56 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
|