Variant #0000472809 (NC_000018.9:g.58039563C>T, NM_005912.2:c.20G>A (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.58039563C>T |
DNA change (hg38) |
g.60372330C>T |
Published as |
- |
ISCN |
- |
DB-ID |
MC4R_000045 See all 4 reported entries |
Variant remarks |
- |
Reference |
PubMed: Xiang et al 2010 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
4.0E-5 View details |
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 |
2011-01-19 10:07:10 +01:00 (CET) |

Variant on transcripts
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