Variant #0000044827 (NC_000016.9:g.3651011G>T, NM_032444.2:c.1132C>A (SLX4))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.3651011G>T
DNA change (hg38) g.3601010G>T
Published as -
ISCN -
DB-ID SLX4_000075 See all 2 reported entries
Variant remarks expression cloning Slx4-deficient MEFs mitomycin C resistant
Reference PubMed: Bakker 2013, Journal: Bakker 2013
ClinVar ID -
dbSNP ID -
Origin Not applicable
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2012-08-31 16:38:57 +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     

Haplotype     
SLX4 NM_032444.2 -?/. 5 c.1132C>A r.(?) p.Pro378Thr -


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