Variant #0000082516 (NC_000005.9:g.177580619_177580635dup, NC_000005.9(NM_017838.3):c.160+43_161-39dup (NHP2))
Chromosome |
5 |
Allele |
Parent #1 |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.177580619_177580635dup |
DNA change (hg38) |
g.178153618_178153634dup |
Published as |
c.160+43_59dup |
ISCN |
- |
DB-ID |
NHP2_000006 |
Variant remarks |
- |
Reference |
PubMed: Vulliamy 2008, Journal: Vulliamy 2008 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
1/117 cases |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2015-10-26 20:36:32 +01:00 (CET) |
Date last edited |
2020-06-18 11:15:12 +02:00 (CEST) |

Variant on transcripts
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