Variant #0000903259 (NC_000005.9:g.176562812G>C, NM_022455.4:c.708G>C (NSD1))

Chromosome 5
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.176562812G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID NSD1_000435 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs28932175
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00015 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-11-24 10:49:01 +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     
NSD1 NM_022455.4 -?/. - c.708G>C r.(?) p.(Gln236His)


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