Variant #0000473156 (NC_000018.9:g.58039207C>A, NM_005912.2:c.376G>T (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.58039207C>A |
DNA change (hg38) |
g.60371974C>A |
Published as |
- |
ISCN |
- |
DB-ID |
MC4R_000075 See all 2 reported entries |
Variant remarks |
- |
Reference |
PubMed: Stutzmann et al 2008 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0 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 14:36:42 +01:00 (CET) |

Variant on transcripts
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