Variant #0000308549 (NC_000016.9:g.3658501T>C, NM_032444.2:c.465A>G (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.3658501T>C
DNA change (hg38) g.3608500T>C
Published as SLX4(NM_032444.2):c.465A>G (p.E155=)
ISCN -
DB-ID SLX4_000011 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) 0.00019 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 2020-07-09 11:20:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
DNASE1 NM_005223.3 -?/. - c.-46546T>C r.(?) p.(=) -
TRAP1 NM_016292.2 -?/. - c.*49629A>G r.(=) p.(=) -
SLX4 NM_032444.2 -?/. - c.465A>G r.(?) p.(Glu155=) -


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