Variant #0001031356 (NC_000001.10:g.156054126_156054127del, NM_170707.3:c.-30584_-30583del (LMNA))

Chromosome 1
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.156054126_156054127del
DNA change (hg38) -
Published as LMNA(NM_001282625.2):c.-319+1151_-319+1152del
ISCN -
DB-ID LMNA_000800
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEX3A NM_001093725.1 -?/. - c.-2337_-2336del r.(?) p.(=)
LMNA NM_170707.3 -?/. - c.-30584_-30583del r.(?) p.(=)


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