Variant #0000334426 (NC_000023.10:g.64738006_64738008del, LAS1L(NM_031206.4):c.1791_1793del)

Chromosome X
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.64738006_64738008del
DNA change (hg38) g.65518126_65518128del
Published as LAS1L(NM_001170649.1):c.1740_1742del (p.(Asp580del)), LAS1L(NM_031206.4):c.1791_1793delTGA (p.D597del)
ISCN -
DB-ID LAS1L_000011 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 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAS1L NM_031206.4 ?/. - c.1791_1793del r.(?) p.(Asp597del)