Variant #0000472756 (NC_000018.9:g.58040022_58040023del, NM_005912.2:c.-439_-438del (MC4R))
Chromosome |
18 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.58040022_58040023del |
DNA change (hg38) |
g.60372789_60372790del |
Published as |
- |
ISCN |
- |
DB-ID |
MC4R_000004 See all 4 reported entries |
Variant remarks |
- |
Reference |
PubMed: Valli-Jaakola et al 2006 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Linda van den Berg |
Database submission license |
No license selected |
Created by |
Linda van den Berg |
Date created |
2010-10-22 15:10:09 +02:00 (CEST) |
Date last edited |
2020-07-15 08:56:34 +02:00 (CEST) |

Variant on transcripts
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