Variant #0000866205 (NC_000019.9:g.48637278G>A, NM_000234.1:c.1569C>T (LIG1))

Chromosome 19
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.48637278G>A
DNA change (hg38) -
Published as LIG1(NM_001320970.1):c.1566C>T (p.H522=), LIG1(NM_001320970.2):c.1566C>T (p.H522=)
ISCN -
DB-ID LIG1_000026 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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LIG1 NM_000234.1 -?/. - c.1569C>T r.(?) p.(His523=)


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