Variant #0000255030 (NC_000019.9:g.48624468A>C, NM_000234.1:c.2344T>G (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.48624468A>C
DNA change (hg38) g.48121211A>C
Published as LIG1(NM_000234.1):c.2344T>G (p.S782A), LIG1(NM_001320970.1):c.2341T>G (p.S781A)
ISCN -
DB-ID LIG1_000001 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) 0.00016 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LIG1 NM_000234.1 -?/. - c.2344T>G r.(?) p.(Ser782Ala)


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