Variant #0000868116 (NC_000005.9:g.176561975del, NSD1(NM_022455.4):c.-17-113del)

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.176561975del
DNA change (hg38) -
Published as -
ISCN -
DB-ID NSD1_000418
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1351511771
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner MobiDetails
Database submission license No license selected
Created by MobiDetails
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NSD1 NM_022455.4 -?/. - c.-17-113del r.(?) p.(?)