Variant #0000609181 (NC_000004.11:g.1940179_1940182del, NM_001042424.2:c.1676_1679del (WHSC1))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1940179_1940182del
DNA change (hg38) g.1938452_1938455del
Published as NSD2(NM_133334.2):c.1675-2_1676delAGAG
ISCN -
DB-ID WHSC1_000012 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WHSC1 NM_001042424.2 +/. - c.1676_1679del r.(?) p.(Arg559ThrfsTer38)


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