Variant #0000282062 (NC_000001.10:g.209801477_209801487del, LAMB3(NM_000228.2):c.1186_1196del)
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.209801477_209801487del |
DNA change (hg38) |
g.209628132_209628142del |
Published as |
LAMB3(NM_001017402.2):c.1186_1196delACCGGGCAGTG (p.T396Cfs*12) |
ISCN |
- |
DB-ID |
LAMB3_000008 |
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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |

Variant on transcripts
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