Variant #0000541151 (NC_000010.10:g.88428507del, LDB3(NM_007078.2):c.59del)
Chromosome |
10 |
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.88428507del |
DNA change (hg38) |
g.86668750del |
Published as |
LDB3(NM_001171610.1):c.59delG (p.G20Afs*41), LDB3(NM_001171610.2):c.59delG (p.G20Afs*41), LDB3(NM_007078.2):c.59del (p.(Gly20AlafsTer41)) |
ISCN |
- |
DB-ID |
LDB3_000106 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) |
Variant not found in online data sets |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |

Variant on transcripts
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