Variant #0000279385 (NC_000005.9:g.126140540G>A, NM_005573.3:c.432G>A (LMNB1))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.126140540G>A
DNA change (hg38) g.126804848G>A
Published as LMNB1(NM_001198557.1):c.-199G>A (p.(=)), LMNB1(NM_005573.4):c.432G>A (p.S144=)
ISCN -
DB-ID LMNB1_000002 See all 3 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) 0.02043 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LMNB1 NM_005573.3 -/. - c.432G>A r.(?) p.(Ser144=)


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