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 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMB3 NM_000228.2 +/. - c.1186_1196del r.(?) p.(Thr396CysfsTer12)