Variant #0000558092 (NC_000016.9:g.3634861G>A, NM_032444.2:c.4648C>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.3634861G>A
DNA change (hg38) g.3584860G>A
Published as SLX4(NM_032444.2):c.4648C>T (p.R1550W, p.(Arg1550Trp)), SLX4(NM_032444.4):c.4648C>T (p.R1550W)
ISCN -
DB-ID SLX4_000028 See all 5 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) 0.00279 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
SLX4 NM_032444.2 -?/. - c.4648C>T r.(?) p.(Arg1550Trp) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.