Variant #0000886248 (NC_000004.11:g.1918721A>T, NM_001042424.2:c.884A>T (WHSC1))

Chromosome 4
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.1918721A>T
DNA change (hg38) -
Published as NSD2(NM_133330.3):c.884A>T (p.Q295L), WHSC1(NM_001042424.2):c.884A>T (p.(Gln295Leu))
ISCN -
DB-ID WHSC1_000032 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) 0.00051 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 2022-11-01 13:01:21 +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     
WHSC1 NM_001042424.2 -?/. - c.884A>T r.(?) p.(Gln295Leu)


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