Variant #0000283549 (NC_000002.11:g.97377734_97377735del, NM_030805.3:c.536_537del (LMAN2L))

Chromosome 2
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.97377734_97377735del
DNA change (hg38) g.96711997_96711998del
Published as LMAN2L(NM_001142292.1):c.569_570delTG (p.V190Efs*8)
ISCN -
DB-ID LMAN2L_000001
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LMAN2L NM_030805.3 ?/. - c.536_537del r.(?) p.(Val179GlufsTer8)


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