Variant #0000726959 (NC_000018.9:g.58038832_58038833del, NM_005912.2:c.750_751del (MC4R))
Chromosome |
18 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.58038832_58038833del |
DNA change (hg38) |
- |
Published as |
MC4R(NM_005912.3):c.750_751delGA (p.I251Wfs*34) |
ISCN |
- |
DB-ID |
MC4R_000149 See all 10 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
4.0E-5 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2021-02-08 18:36:18 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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