Variant #0000951263 (NC_000019.9:g.2431810G>A, NM_032737.3:c.1681C>T (LMNB2))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2431810G>A
DNA change (hg38) -
Published as LMNB2(NM_032737.4):c.1681C>T (p.R561C)
ISCN -
DB-ID LMNB2_000003
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) 0.00014 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LMNB2 NM_032737.3 ?/. - c.1681C>T r.(?) p.(Arg561Cys)
TMPRSS9 NM_182973.1 ?/. - c.*5724G>A r.(=) p.(=)


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