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 |

Variant on transcripts
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