Variant #0000452222 (NC_000001.10:g.156108352G>T, NM_170707.3:c.1772G>T (LMNA))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.156108352G>T
DNA change (hg38) g.156138561G>T
Published as -
ISCN -
DB-ID LMNA_000228 See all 3 reported entries
Variant remarks cloned in pCMV6-XL5-FLAG, expressed in 3T3-L1 preadipocytes, enlarged nucleus (15%), invaginations, LMNA aggregation
Reference PubMed: Araujo-Vilar 2008
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner David Araujo-Vilar
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-09-26 21:22:36 +02:00 (CEST)
Date last edited 2020-07-14 21:57:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LMNA NM_170707.3 +/. 11 c.1772G>T r.(?) p.Cys591Phe


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