Variant #0001041101 (NC_000016.9:g.3658876G>A, NM_032444.2:c.90C>T (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.3658876G>A
DNA change (hg38) -
Published as SLX4(NM_032444.4):c.90C>T (p.(Ser30=), p.S30=)
ISCN -
DB-ID SLX4_000012 See all 3 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) 0.006 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
DNASE1 NM_005223.3 -/. - c.-46171G>A r.(?) p.(=) -
TRAP1 NM_016292.2 -/. - c.*49254C>T r.(=) p.(=) -
SLX4 NM_032444.2 -/. - c.90C>T r.(?) p.(Ser30=) -


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