Variant #0000655253 (NC_000005.9:g.126141392_126141395dup, NC_000005.9(NM_005573.3):c.642+4_642+7dup (LMNB1))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.126141392_126141395dup
DNA change (hg38) g.126805700_126805703dup
Published as LMNB1(NM_005573.3):c.642+2_642+5dupTAAC
ISCN -
DB-ID LMNB1_000020
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-17 14:57:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LMNB1 NM_005573.3 -?/. - c.642+4_642+7dup r.spl? p.?


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