Variant #0000549734 (NC_000013.10:g.108862111_108862112del, NM_002312.3:c.1512_1513del (LIG4))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.108862111_108862112del
DNA change (hg38) g.108209763_108209764del
Published as LIG4(NM_002312.3):c.1512_1513delTC (p.R505Cfs*12)
ISCN -
DB-ID LIG4_000007 See all 2 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-04 14:28:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LIG4 NM_002312.3 +/. - c.1512_1513del r.(?) p.(Arg505CysfsTer12)


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