Variant #0001026705 (NC_000016.9:g.3658544C>A, NM_032444.2:c.422G>T (SLX4))

Chromosome 16
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.3658544C>A
DNA change (hg38) -
Published as SLX4(NM_032444.4):c.422G>T (p.G141V)
ISCN -
DB-ID DNASE1_000088
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) 0.00032 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-02-07 18:57:27 +01:00 (CET)
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.-46503C>A r.(?) p.(=) -
TRAP1 NM_016292.2 -?/. - c.*49586G>T r.(=) p.(=) -
SLX4 NM_032444.2 -?/. - c.422G>T r.(?) p.(Gly141Val) -


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