Variant #0000549732 (NC_000013.10:g.108861663C>T, NM_002312.3:c.1954G>A (LIG4))

Chromosome 13
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.108861663C>T
DNA change (hg38) g.108209315C>T
Published as LIG4(NM_001352599.2):c.1954G>A (p.V652I), LIG4(NM_002312.3):c.1954G>A (p.V652I)
ISCN -
DB-ID LIG4_000029 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) 2.0E-5 View details
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 2021-09-17 14:40:49 +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.1954G>A r.(?) p.(Val652Ile)


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